C-Nucleophiles

For reactivities of structurally related compounds go to: Nucleophiles

Found 572 Molecules.

Molecule	Solvent	Reactivity Parameters	Reference (sort by title or year)
Z-3-(trimethylsiloxy)pent-2-ene	dichloromethane	N Parameter: 5.58 s_N Parameter: 1.00	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
trimethyl(prenyl)silane	dichloromethane	N Parameter: 0.90 s_N Parameter: 1.17	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
toluene	dichloromethane	N Parameter: -4.36 s_N Parameter: 1.77	J. Am. Chem. Soc. 2012, 134, 13902-13911 DOI: 10.1021/ja306522b
thiophene	dichloromethane	N Parameter: -1.01 s_N Parameter: 1.10	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
tetramethylethylene	dichloromethane	N Parameter: -1.00 s_N Parameter: 1.40	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
tetrakis(5-methyl-furan-2-yl)borate	MeCN	N Parameter: 9.09 s_N Parameter: 1.12	Chem. Sci. 2012, 3, 878-882 DOI: 10.1039/c2sc00883a
tert-butyl isocyanide	dichloromethane	N Parameter: 5.47 s_N Parameter: 0.77	Angew. Chem. Int. Ed. 2007, 46, 3563-3566 DOI: 10.1002/anie.200605205
tert-butyl indole-1-carboxylate	MeCN	N Parameter: 1.68 s_N Parameter: 1.26	J. Am. Chem. Soc. 2013, 135, 6317-6324 DOI: 10.1021/ja4017655
styrene	dichloromethane	N Parameter: 0.78 s_N Parameter: 0.95	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
sodium indenide (in DMSO)	DMSO	N Parameter: 23.74 s_N Parameter: 0.71	Angew. Chem. Int. Ed. 2015, 54, 12497-12500 DOI: 10.1002/anie.201501385
pyrrole	dichloromethane	N Parameter: 4.63 s_N Parameter: 1.00	Chem. Eur. J. 2003, 9, 2209-2218 DOI: 10.1002/chem.200204666
propene	dichloromethane	N Parameter: -2.41 s_N Parameter: 1.00	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
prenyl-tributylstannane	dichloromethane	N Parameter: 4.74 s_N Parameter: 1.15	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
potassium trifluoro(furan-3-yl)borate	MeCN	N Parameter: 6.83 s_N Parameter: 0.93	J. Am. Chem. Soc. 2013, 135, 6317-6324 DOI: 10.1021/ja4017655
potassium trifluoro(3-methoxy-thiophen-2-yl)borate	MeCN	N Parameter: 7.32 s_N Parameter: 0.90	J. Am. Chem. Soc. 2013, 135, 6317-6324 DOI: 10.1021/ja4017655
potassium trifluoro(1-methyl-1H-indol-5-yl)borate	MeCN	N Parameter: 8.77 s_N Parameter: 1.09	J. Am. Chem. Soc. 2013, 135, 6317-6324 DOI: 10.1021/ja4017655
potassium trifluoro(1-methyl-1H-indol-2-yl)borate	MeCN	N Parameter: 9.55 s_N Parameter: 1.16	J. Am. Chem. Soc. 2013, 135, 6317-6324 DOI: 10.1021/ja4017655
potassium indenide (in DMSO)	DMSO	N Parameter: 24.16 s_N Parameter: 0.68	Angew. Chem. Int. Ed. 2015, 54, 12497-12500 DOI: 10.1002/anie.201501385
potassium allyltrifluoroborate (in MeCN)	MeCN	N Parameter: 5.29 s_N Parameter: 0.87	J. Am. Chem. Soc. 2017, 139, 15324-15327 DOI: 10.1021/jacs.7b10240
potassium (1-(tert-butoxycarbonyl)-5-methoxy-1H-indol-2-yl)trifluoroborate	MeCN	N Parameter: 7.10 s_N Parameter: 1.18	J. Am. Chem. Soc. 2013, 135, 6317-6324 DOI: 10.1021/ja4017655
potassium (1-(tert-butoxycarbonyl)-1H-indol-3-yl)trifluoroborate	MeCN	N Parameter: 4.06 s_N Parameter: 0.79	J. Am. Chem. Soc. 2013, 135, 6317-6324 DOI: 10.1021/ja4017655
potassium (1-(tert-butoxycarbonyl)-1H-indol-2-yl)trifluoroborate	MeCN	N Parameter: 6.46 s_N Parameter: 0.96	J. Am. Chem. Soc. 2013, 135, 6317-6324 DOI: 10.1021/ja4017655
phenyldiazomethane	dichloromethane	N Parameter: 9.35 s_N Parameter: 0.83	Chem. Eur. J. 2003, 9, 4068-4076 DOI: 10.1002/chem.200304913
phenylacetylene	dichloromethane	N Parameter: -0.04 s_N Parameter: 0.77	Angew. Chem. Int. Ed. 2014, 53, 4968-4971 DOI: 10.1002/anie.201402055
Ph3P=CH-COPh	dichloromethane	N Parameter: 9.54 s_N Parameter: 0.97	J. Am. Chem. Soc. 2009, 131, 704-714 DOI: 10.1021/ja8056216
Ph3P=CH-CO2Et (in DMSO)	DMSO	N Parameter: 12.21 s_N Parameter: 0.62	J. Am. Chem. Soc. 2009, 131, 704-714 DOI: 10.1021/ja8056216
Ph3P=CH-CO2Et	dichloromethane	N Parameter: 12.79 s_N Parameter: 0.77	J. Am. Chem. Soc. 2009, 131, 704-714 DOI: 10.1021/ja8056216
Ph3P=CH-CN	dichloromethane	N Parameter: 12.29 s_N Parameter: 0.75	J. Am. Chem. Soc. 2009, 131, 704-714 DOI: 10.1021/ja8056216
Ph3P=CH-CHO (in MeCN)	MeCN	N Parameter: 9.09 s_N Parameter: 0.74	J. Am. Chem. Soc. 2016, 138, 11272-11281 DOI: 10.1021/jacs.6b06264
Ph3P=CH-C(O)Me (in MeCN)	MeCN	N Parameter: 10.27 s_N Parameter: 0.83	J. Am. Chem. Soc. 2016, 138, 11272-11281 DOI: 10.1021/jacs.6b06264
Ph3P=C(CH3)-CO2Et	dichloromethane	N Parameter: 13.09 s_N Parameter: 0.73	J. Am. Chem. Soc. 2009, 131, 704-714 DOI: 10.1021/ja8056216
Ph2P(O)CH(-)CO2Et (in DMSO)	DMSO	N Parameter: 19.20 s_N Parameter: 0.69	J. Am. Chem. Soc. 2009, 131, 704-714 DOI: 10.1021/ja8056216
Ph2P(O)CH(-)CN (in DMSO)	DMSO	N Parameter: 18.69 s_N Parameter: 0.72	J. Am. Chem. Soc. 2009, 131, 704-714 DOI: 10.1021/ja8056216
p-tosylmethyl isocyanide (TosMIC)	dichloromethane	N Parameter: 3.50 s_N Parameter: 0.76	Angew. Chem. Int. Ed. 2007, 46, 3563-3566 DOI: 10.1002/anie.200605205
norbornene	dichloromethane	N Parameter: -0.25 s_N Parameter: 1.09	J. Am. Chem. Soc. 2012, 134, 13902-13911 DOI: 10.1021/ja306522b
N-vinylcarbazole	dichloromethane	N Parameter: 5.02 s_N Parameter: 0.94	Macromolecules 2002, 35, 5454-5458 DOI: 10.1021/ma020306l
N-methylpyrrole	dichloromethane	N Parameter: 5.85 s_N Parameter: 1.03	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
N-methylindole	dichloromethane	N Parameter: 5.75 s_N Parameter: 1.23	J. Org. Chem. 2006, 71, 9088-9095 DOI: 10.1021/jo0614339
N-methylenepyrrolidin-1-amine (in CH2Cl2)	dichloromethane	N Parameter: 7.84 s_N Parameter: 0.89	Angew. Chem. Int. Ed. 2013, 52, 11900-11904 DOI: 10.1002/anie.201305092
n-butyl vinyl ether	dichloromethane	N Parameter: 3.76 s_N Parameter: 0.91	J. Am. Chem. Soc. 2012, 134, 13902-13911 DOI: 10.1021/ja306522b
N-benzyl-N-(but-1-yn-1-yl)-4-methylbenzenesulfonamide	dichloromethane	N Parameter: 5.16 s_N Parameter: 0.85	Angew. Chem. Int. Ed. 2014, 53, 4968-4971 DOI: 10.1002/anie.201402055
N-benzyl-N-((2-methoxyphenyl)ethynyl)-4-methylbenzenesulfonamide	dichloromethane	N Parameter: 4.40 s_N Parameter: 0.86	Angew. Chem. Int. Ed. 2014, 53, 4968-4971 DOI: 10.1002/anie.201402055
N-(triisopropylsilyl)pyrrole	dichloromethane	N Parameter: 3.12 s_N Parameter: 0.93	Chem. Eur. J. 2003, 9, 2209-2218 DOI: 10.1002/chem.200204666
N-(cyclopent-1-en-1-yl)acetamide	MeCN	N Parameter: 7.06 s_N Parameter: 0.87	Chem. Eur. J. 2012, 18, 5732-5740 DOI: 10.1002/chem.201103519
N-(cyclohex-1-en-1-yl)acetamide	MeCN	N Parameter: 5.64 s_N Parameter: 0.79	Chem. Eur. J. 2012, 18, 5732-5740 DOI: 10.1002/chem.201103519
N-(3,4-dihydronaphthalen-1-yl)acetamide	MeCN	N Parameter: 4.91 s_N Parameter: 0.87	Chem. Eur. J. 2012, 18, 5732-5740 DOI: 10.1002/chem.201103519
N-(3,3-dimethylbut-1-en-2-yl)acetamide	MeCN	N Parameter: 4.61 s_N Parameter: 0.98	Chem. Eur. J. 2012, 18, 5732-5740 DOI: 10.1002/chem.201103519
N-(1-phenylvinyl)benzamide	MeCN	N Parameter: 5.44 s_N Parameter: 1.00	Chem. Eur. J. 2012, 18, 5732-5740 DOI: 10.1002/chem.201103519
N-(1-phenylvinyl)acetamide	MeCN	N Parameter: 5.73 s_N Parameter: 0.97	Chem. Eur. J. 2012, 18, 5732-5740 DOI: 10.1002/chem.201103519
N-(1-(p-tolyl)vinyl)acetamide	MeCN	N Parameter: 6.57 s_N Parameter: 0.91	Chem. Eur. J. 2012, 18, 5732-5740 DOI: 10.1002/chem.201103519
N-(1-(naphthalen-2-yl)vinyl)acetamide	MeCN	N Parameter: 6.28 s_N Parameter: 0.95	Chem. Eur. J. 2012, 18, 5732-5740 DOI: 10.1002/chem.201103519
N-(1-(4-methoxyphenyl)vinyl)acetamide	MeCN	N Parameter: 7.06 s_N Parameter: 0.85	Chem. Eur. J. 2012, 18, 5732-5740 DOI: 10.1002/chem.201103519
N-(1-(4-chlorophenyl)vinyl)acetamide	MeCN	N Parameter: 5.60 s_N Parameter: 1.00	Chem. Eur. J. 2012, 18, 5732-5740 DOI: 10.1002/chem.201103519
N,N-Dimethylbarbituric acid iodonium ylide (in CHCl2)	dichloromethane	N Parameter: 7.98 s_N Parameter: 0.71	J. Am. Chem. Soc. 2016, 138, 10304-10313 DOI: 10.1021/jacs.6b05768
morpholinoisobutylene	dichloromethane	N Parameter: 10.04 s_N Parameter: 0.82	Chem. Eur. J. 2003, 9, 2209-2218 DOI: 10.1002/chem.200204666
methylenecycloundecane	dichloromethane	N Parameter: 2.33 s_N Parameter: 0.90	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
methylenecyclopropane	dichloromethane	N Parameter: -0.47 s_N Parameter: 0.90	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
methylenecyclopentane	dichloromethane	N Parameter: 2.82 s_N Parameter: 0.90	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
methylenecyclopentadecane	dichloromethane	N Parameter: 1.69 s_N Parameter: 0.90	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
methylenecyclooctane	dichloromethane	N Parameter: 3.16 s_N Parameter: 0.90	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
methylenecyclononane	dichloromethane	N Parameter: 2.57 s_N Parameter: 0.90	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
methylenecyclohexane	dichloromethane	N Parameter: 1.16 s_N Parameter: 1.04	J. Am. Chem. Soc. 2012, 134, 13902-13911 DOI: 10.1021/ja306522b
methylenecycloheptane	dichloromethane	N Parameter: 2.24 s_N Parameter: 0.90	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
methylenecyclododecane	dichloromethane	N Parameter: 1.52 s_N Parameter: 0.90	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
methylenecyclodecane	dichloromethane	N Parameter: 2.82 s_N Parameter: 0.90	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
methylenecyclobutane	dichloromethane	N Parameter: 1.65 s_N Parameter: 0.90	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
methyl diazoacetate	dichloromethane	N Parameter: 4.68 s_N Parameter: 0.94	J. Am. Chem. Soc. 2023, 145, 7416-7434 DOI: 10.1021/jacs.2c13872
methyl (cyclohexen-1-yl)prolinate (in MeCN)	MeCN	N Parameter: 14.96 s_N Parameter: 0.68	Angew. Chem. Int. Ed. 2010, 49, 9526-9529 DOI: 10.1002/anie.201004344
methoxybis(phenylsulfonyl)methanide (in DMSO)	DMSO	N Parameter: 17.29 s_N Parameter: 0.70	Angew. Chem. Int. Ed. 2016, 55, 12845-12848 DOI: 10.1002/anie.201605616
MeSO2-CH-CO2Et (in DMSO)	DMSO	N Parameter: 18.00 s_N Parameter: 0.66	Chem. Eur. J. 2010, 16, 8610-8614 DOI: 10.1002/chem.201001455
MeSO-CH-CO2Et (in DMSO)	DMSO	N Parameter: 20.61 s_N Parameter: 0.64	Chem. Eur. J. 2010, 16, 8610-8614 DOI: 10.1002/chem.201001455
MeO-Breslow 1e	THF	N Parameter: 15.65 s_N Parameter: 0.52	Angew. Chem. Int. Ed. 2012, 51, 10408-10412 DOI: 10.1002/anie.201204524
MeO-Breslow 1c	THF	N Parameter: 16.61 s_N Parameter: 0.68	Angew. Chem. Int. Ed. 2012, 51, 10408-10412 DOI: 10.1002/anie.201204524
MeO-Breslow 1b	THF	N Parameter: 10.45 s_N Parameter: 0.81	Angew. Chem. Int. Ed. 2012, 51, 10408-10412 DOI: 10.1002/anie.201204524
MeO-Breslow 1a	THF	N Parameter: 14.77 s_N Parameter: 0.80	Angew. Chem. Int. Ed. 2012, 51, 10408-10412 DOI: 10.1002/anie.201204524
Meldrum's acid iodonium ylide (in CH2Cl2)	dichloromethane	N Parameter: 4.36 s_N Parameter: 1.06	J. Am. Chem. Soc. 2016, 138, 10304-10313 DOI: 10.1021/jacs.6b05768
Me2S=CH-CO2Et (in DMSO)	DMSO	N Parameter: 15.85 s_N Parameter: 0.61	Chem. Eur. J. 2010, 16, 8610-8614 DOI: 10.1002/chem.201001455
Me2S=CH-CN (in DMSO)	DMSO	N Parameter: 16.23 s_N Parameter: 0.60	Chem. Eur. J. 2010, 16, 8610-8614 DOI: 10.1002/chem.201001455
Me2S=CH(p-NO2-C6H4) (in DMSO)	DMSO	N Parameter: 18.42 s_N Parameter: 0.65	J. Am. Chem. Soc. 2010, 132, 17894-17900 DOI: 10.1021/ja1084749
Me2S=CH(4-CN-C6H4) (in DMSO)	DMSO	N Parameter: 21.07 s_N Parameter: 0.68	J. Am. Chem. Soc. 2010, 132, 17894-17900 DOI: 10.1021/ja1084749
Me2S(O)=CH2 (in DMSO)	DMSO	N Parameter: 21.29 s_N Parameter: 0.47	J. Am. Chem. Soc. 2010, 132, 17894-17900 DOI: 10.1021/ja1084749
m-xylene	dichloromethane	N Parameter: -3.57 s_N Parameter: 2.08	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
lithium indenide (in DMSO)	DMSO	N Parameter: 23.66 s_N Parameter: 0.70	Angew. Chem. Int. Ed. 2015, 54, 12497-12500 DOI: 10.1002/anie.201501385
lithium bis(5-methylthiophen-2-yl)pinacolborate	MeCN	N Parameter: 7.67 s_N Parameter: 0.87	Angew. Chem. Int. Ed. 2015, 54, 2780-2783 DOI: 10.1002/anie.201410562
lithium 5,5-dimethyl-2-(1-phenylethyl)-2-(4-(trifluoromethyl)phenyl)-1,3,2-dioxaborinan-2-uide (in MeCN)	MeCN	N Parameter: 11.29 s_N Parameter: 0.76	Org. Lett. 2015, 17, 2614-2617 DOI: 10.1021/acs.orglett.5b00918
lithium 4,4,5,5-tetramethyl-2-phenyl-2-(prop-1-en-2-yl)-1,3,2-dioxaborolan-2-uide (in MeCN)	MeCN	N Parameter: 11.00 s_N Parameter: 0.57	J. Am. Chem. Soc. 2022, 144, 16118-16130 DOI: 10.1021/jacs.2c06493
lithium 4,4,5,5-tetramethyl-2-phenyl-2-(1-phenylethyl)-1,3,2-dioxaborolan-2-uide (in MeCN)	MeCN	N Parameter: 10.97 s_N Parameter: 0.63	Org. Lett. 2015, 17, 2614-2617 DOI: 10.1021/acs.orglett.5b00918
lithium 4,4,5,5-tetramethyl-2-(1-phenylethyl)-2-(4-(trifluoromethyl)phenyl)-1,3,2-dioxaborolan-2-uide (in MeCN)	MeCN	N Parameter: 8.56 s_N Parameter: 0.76	Org. Lett. 2015, 17, 2614-2617 DOI: 10.1021/acs.orglett.5b00918
lithium 2-isopropyl-4,4,5,5-tetramethyl-2-(4-(trifluoromethyl)phenyl)-1,3,2-dioxaborolan-2-uide (in MeCN)	MeCN	N Parameter: 6.63 s_N Parameter: 0.75	Org. Lett. 2015, 17, 2614-2617 DOI: 10.1021/acs.orglett.5b00918
lithium 2-ethyl-4,4,5,5-tetramethyl-2-(4-(trifluoromethyl)phenyl)-1,3,2-dioxaborolan-2-uide (in MeCN)	MeCN	N Parameter: 7.68 s_N Parameter: 0.78	Org. Lett. 2015, 17, 2614-2617 DOI: 10.1021/acs.orglett.5b00918
lithium 2-cyclopropyl-4,4,5,5-tetramethyl-2-(4-(trifluoromethyl)phenyl)-1,3,2-dioxaborolan-2-uide (in MeCN)	MeCN	N Parameter: 7.72 s_N Parameter: 0.75	Org. Lett. 2015, 17, 2614-2617 DOI: 10.1021/acs.orglett.5b00918
lithium 2-benzyl-4,4,5,5-tetramethyl-2-phenyl-1,3,2-dioxaborolan-2-uide (in MeCN)	MeCN	N Parameter: 8.92 s_N Parameter: 0.70	Org. Lett. 2015, 17, 2614-2617 DOI: 10.1021/acs.orglett.5b00918
lithium 2-benzyl-4,4,5,5-tetramethyl-2-(4-(trifluoromethyl)phenyl)-1,3,2-dioxaborolan-2-uide (in MeCN)	MeCN	N Parameter: 7.15 s_N Parameter: 0.77	Org. Lett. 2015, 17, 2614-2617 DOI: 10.1021/acs.orglett.5b00918
lithium 2-benzyl-2-(3,5-bis(trifluoromethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-uide (in MeCN)	MeCN	N Parameter: 6.30 s_N Parameter: 0.78	Org. Lett. 2015, 17, 2614-2617 DOI: 10.1021/acs.orglett.5b00918
lithium 2-allyl-4,4,5,5-tetramethyl-2-phenyl-1,3,2-dioxaborolan-2-uide (in MeCN)	MeCN	N Parameter: 11.20 s_N Parameter: 0.64	J. Am. Chem. Soc. 2017, 139, 15324-15327 DOI: 10.1021/jacs.7b10240
lithium 2-allyl-2-(3,5-bis(trifluoromethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-uide (in MeCN)	MeCN	N Parameter: 8.71 s_N Parameter: 0.80	J. Am. Chem. Soc. 2017, 139, 15324-15327 DOI: 10.1021/jacs.7b10240
lithium 2-(3,5-bis(trifluoromethyl)phenyl)-4,4,5,5-tetramethyl-2-(1-phenylethyl)-1,3,2-dioxaborolan-2-uide (in MeCN)	MeCN	N Parameter: 7.46 s_N Parameter: 0.76	Org. Lett. 2015, 17, 2614-2617 DOI: 10.1021/acs.orglett.5b00918
lithium (E)-2-(3,5-bis(trifluoromethyl)phenyl)-2-(but-2-en-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-uide (in MeCN)	MeCN	N Parameter: 9.49 s_N Parameter: 0.82	J. Am. Chem. Soc. 2017, 139, 15324-15327 DOI: 10.1021/jacs.7b10240
lithium (5-methylthiophen-2-yl)(phenyl)pinacolborate	MeCN	N Parameter: 7.24 s_N Parameter: 0.83	Angew. Chem. Int. Ed. 2015, 54, 2780-2783 DOI: 10.1002/anie.201410562
lithium (5-methylthiophen-2-yl)(4-methylphenyl)pinacolborate	MeCN	N Parameter: 6.98 s_N Parameter: 0.93	Angew. Chem. Int. Ed. 2015, 54, 2780-2783 DOI: 10.1002/anie.201410562
lithium (5-methylthiophen-2-yl)(4-methoxyphenyl)pinacolborate	MeCN	N Parameter: 7.51 s_N Parameter: 0.87	Angew. Chem. Int. Ed. 2015, 54, 2780-2783 DOI: 10.1002/anie.201410562
lithium (5-methylthiophen-2-yl)(4-chlorophenyl)pinacolborate	MeCN	N Parameter: 6.77 s_N Parameter: 0.88	Angew. Chem. Int. Ed. 2015, 54, 2780-2783 DOI: 10.1002/anie.201410562
lithium (5-methylthiophen-2-yl)(4-(trifluoromethyl)phenyl)neopentylglycolborate	MeCN	N Parameter: 11.85 s_N Parameter: 0.72	Angew. Chem. Int. Ed. 2015, 54, 2780-2783 DOI: 10.1002/anie.201410562
lithium (5-methylthiophen-2-yl)(4-(trifluoromethyl)phenyl)catecholglycolborate	MeCN	N Parameter: 6.50 s_N Parameter: 0.77	Angew. Chem. Int. Ed. 2015, 54, 2780-2783 DOI: 10.1002/anie.201410562
lithium (5-methylthiophen-2-yl)(4-(dimethylamino)phenyl)pinacolborate	MeCN	N Parameter: 8.02 s_N Parameter: 0.89	Angew. Chem. Int. Ed. 2015, 54, 2780-2783 DOI: 10.1002/anie.201410562
lithium (5-methylthiophen-2-yl)(3,5-bis(trifluoromethyl)phenyl)pinacolborate	MeCN	N Parameter: 5.53 s_N Parameter: 1.00	Angew. Chem. Int. Ed. 2015, 54, 2780-2783 DOI: 10.1002/anie.201410562
lithium (5-methylthiophen-2-yl)(3,5-bis(trifluoromethyl)phenyl)neopentylglycolborate	MeCN	N Parameter: 10.13 s_N Parameter: 0.91	Angew. Chem. Int. Ed. 2015, 54, 2780-2783 DOI: 10.1002/anie.201410562
lithium (5-methylthiophen-2-yl)(3,5-bis(trifluoromethyl)phenyl)glycolborate	MeCN	N Parameter: 11.23 s_N Parameter: 0.77	Angew. Chem. Int. Ed. 2015, 54, 2780-2783 DOI: 10.1002/anie.201410562
lithium (5-methylfuran-2-yl)(4-(trifluoromethyl)phenyl)pinacolborate	MeCN	N Parameter: 8.13 s_N Parameter: 0.85	Angew. Chem. Int. Ed. 2015, 54, 2780-2783 DOI: 10.1002/anie.201410562
isobutylenyl-ethylether	dichloromethane	N Parameter: 4.23 s_N Parameter: 1.00	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
Indole	dichloromethane	N Parameter: 5.55 s_N Parameter: 1.09	J. Org. Chem. 2006, 71, 9088-9095 DOI: 10.1021/jo0614339
furan	dichloromethane	N Parameter: 1.33 s_N Parameter: 1.29	J. Am. Chem. Soc. 2012, 134, 13902-13911 DOI: 10.1021/ja306522b
fluorobis(phenylsulfonyl)methanide (in DMSO)	DMSO	N Parameter: 17.46 s_N Parameter: 0.73	Angew. Chem. Int. Ed. 2016, 55, 12845-12848 DOI: 10.1002/anie.201605616
ethyl-vinylether	dichloromethane	N Parameter: 3.92 s_N Parameter: 0.90	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
ethyl diazoacetate	dichloromethane	N Parameter: 4.91 s_N Parameter: 0.95	Chem. Eur. J. 2003, 9, 4068-4076 DOI: 10.1002/chem.200304913
ethyl (E)-3-(N-morpholino)acrylate	dichloromethane	N Parameter: 8.52 s_N Parameter: 0.80	Chem. Eur. J. 2003, 9, 2209-2218 DOI: 10.1002/chem.200204666
ethyl (E)-3-(dimethylamino)acrylate	dichloromethane	N Parameter: 9.43 s_N Parameter: 0.80	Chem. Eur. J. 2003, 9, 2209-2218 DOI: 10.1002/chem.200204666
enolate of 3-isochromanone (in DMSO)	DMSO	N Parameter: 25.39 s_N Parameter: 0.54	J. Org. Chem. 2024, 89, 6915-6928 DOI: 10.1021/acs.joc.4c00277
enolate of 2-coumaranone (in DMSO)	DMSO	N Parameter: 19.60 s_N Parameter: 0.75	J. Org. Chem. 2024, 89, 6915-6928 DOI: 10.1021/acs.joc.4c00277
diphenyldiazomethane	dichloromethane	N Parameter: 5.29 s_N Parameter: 0.92	Chem. Eur. J. 2003, 9, 4068-4076 DOI: 10.1002/chem.200304913
dimethyl diazomalonate	dichloromethane	N Parameter: -1.24 s_N Parameter: 0.81	Angew. Chem. Int. Ed. Engl. 1994, 33, 938-957 DOI: 10.1002/anie.199409381
Dimethyl bis(indenyl)zirconium(IV)	dichloromethane	N Parameter: 6.89 s_N Parameter: 1.00	Chem. Eur. J. 2016, 22, 11196-11200 DOI: 10.1002/chem.201602452
Dimethyl 1,1'-isopropylidenezirconocene	dichloromethane	N Parameter: 5.20 s_N Parameter: 1.00	Chem. Eur. J. 2016, 22, 11196-11200 DOI: 10.1002/chem.201602452
Dimedone iodonium ylide (in CH2Cl2)	dichloromethane	N Parameter: 6.18 s_N Parameter: 0.81	J. Am. Chem. Soc. 2016, 138, 10304-10313 DOI: 10.1021/jacs.6b05768
diethyl diazomalonate	dichloromethane	N Parameter: -0.35 s_N Parameter: 0.93	Chem. Eur. J. 2003, 9, 4068-4076 DOI: 10.1002/chem.200304913
diazomethane	dichloromethane	N Parameter: 10.48 s_N Parameter: 0.78	Chem. Eur. J. 2003, 9, 4068-4076 DOI: 10.1002/chem.200304913
diazocyclopentadiene (in CH2Cl2)	dichloromethane	N Parameter: 4.84 s_N Parameter: 1.06	Synthesis 2023, 55, 354-358 DOI: 10.1055/s-0041-1737327
diazoacetone	dichloromethane	N Parameter: 3.96 s_N Parameter: 0.91	Chem. Eur. J. 2003, 9, 4068-4076 DOI: 10.1002/chem.200304913
Dexoxy Breslow intermediate 6	THF	N Parameter: 15.58 s_N Parameter: 0.57	Angew. Chem. Int. Ed. 2012, 51, 10408-10412 DOI: 10.1002/anie.201204524
Desoxy Breslow intermediate 2c'	THF	N Parameter: 12.75 s_N Parameter: 0.71	Angew. Chem. Int. Ed. 2012, 51, 6231-6235 DOI: 10.1002/anie.201202327
Desoxy Breslow intermediate 2b'	THF	N Parameter: 11.42 s_N Parameter: 0.70	Angew. Chem. Int. Ed. 2012, 51, 6231-6235 DOI: 10.1002/anie.201202327
Desoxy Breslow intermediate 2b	THF	N Parameter: 13.91 s_N Parameter: 0.64	Angew. Chem. Int. Ed. 2012, 51, 6231-6235 DOI: 10.1002/anie.201202327
Desoxy Breslow intermediate 2a'	THF	N Parameter: 14.45 s_N Parameter: 0.71	Angew. Chem. Int. Ed. 2012, 51, 6231-6235 DOI: 10.1002/anie.201202327
Desoxy Breslow intermediate 2a	THF	N Parameter: 17.12 s_N Parameter: 0.80	Angew. Chem. Int. Ed. 2012, 51, 6231-6235 DOI: 10.1002/anie.201202327
Desoxy Breslow intermediate 2a	DMSO	N Parameter: 17.41 s_N Parameter: 0.74	Angew. Chem. Int. Ed. 2012, 51, 6231-6235 DOI: 10.1002/anie.201202327
Danishefskys diene	dichloromethane	N Parameter: 8.57 s_N Parameter: 0.84	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
cyclopentene	dichloromethane	N Parameter: -1.55 s_N Parameter: 1.10	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
cyclopentadiene	dichloromethane	N Parameter: 2.30 s_N Parameter: 1.06	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
cycloocta-1,3-diene	dichloromethane	N Parameter: -0.50 s_N Parameter: 1.10	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
cyclohexa-1,3-diene	dichloromethane	N Parameter: 0.67 s_N Parameter: 1.10	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
cyclohepta-1,3-diene	dichloromethane	N Parameter: 0.06 s_N Parameter: 1.10	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
cyclohepta-1,3,5-trienyl-Fe(CO)3	dichloromethane	N Parameter: 3.42 s_N Parameter: 0.94	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
cyano(pyridin-1-ium-1-yl)methanide (in DMSO)	DMSO	N Parameter: 25.94 s_N Parameter: 0.42	J. Am. Chem. Soc. 2013, 135, 15216-15224 DOI: 10.1021/ja407885h
cyano((diphenylmethylene)amino)methanide	DMSO	N Parameter: 29.50 s_N Parameter: 0.50	Tetrahedron 2019, 75, 459-463 DOI: 10.1016/j.tet.2018.11.075
cyanide (in MeCN)	MeCN	N Parameter: 16.27 s_N Parameter: 0.70	Angew. Chem. Int. Ed. 2005, 44, 142-145 DOI: 10.1002/anie.200461640
Cp2Zr(Me)2 - Dimethylzirconocene	dichloromethane	N Parameter: 4.35 s_N Parameter: 1.09	Chem. Eur. J. 2016, 22, 11196-11200 DOI: 10.1002/chem.201602452
Cp2Zr(CH2Ph)2 - Dibenzylzirconocene	dichloromethane	N Parameter: 5.10 s_N Parameter: 1.03	Chem. Eur. J. 2016, 22, 11196-11200 DOI: 10.1002/chem.201602452
Cp2Ti(CH2Ph)2 - Dibenzyltitanocene	dichloromethane	N Parameter: 4.38 s_N Parameter: 1.00	Chem. Eur. J. 2016, 22, 11196-11200 DOI: 10.1002/chem.201602452
chloro(phenylsulfonyl)methanide (in DMSO)	DMSO	N Parameter: 28.27 s_N Parameter: 0.42	J. Org. Chem. 2017, 82, 2011-2017 DOI: 10.1021/acs.joc.6b02844
chloro(phenylsulfonyl)methanide (in DMF)	DMF	N Parameter: 26.64 s_N Parameter: 0.64	Chem. Eur. J. 2008, 14, 6108-6118 DOI: 10.1002/chem.200800329
chloro((4-nitrophenyl)sulfonyl)methanide (in DMSO)	DMSO	N Parameter: 24.88 s_N Parameter: 0.49	J. Org. Chem. 2017, 82, 2011-2017 DOI: 10.1021/acs.joc.6b02844
chloro((4-cyanophenyl)sulfonyl)methanide (in DMSO)	DMSO	N Parameter: 25.59 s_N Parameter: 0.51	J. Org. Chem. 2017, 82, 2011-2017 DOI: 10.1021/acs.joc.6b02844
chloro((4-chlorophenyl)sulfonyl)methanide (in DMSO)	DMSO	N Parameter: 26.90 s_N Parameter: 0.45	J. Org. Chem. 2017, 82, 2011-2017 DOI: 10.1021/acs.joc.6b02844
buta-1,3-diene	dichloromethane	N Parameter: -0.87 s_N Parameter: 1.00	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
bromo(phenylsulfonyl)methanide (in DMSO)	DMSO	N Parameter: 23.90 s_N Parameter: 0.62	J. Org. Chem. 2017, 82, 2011-2017 DOI: 10.1021/acs.joc.6b02844
bis(phenylsulfonyl)methanide (in DMSO)	DMSO	N Parameter: 15.68 s_N Parameter: 0.74	Angew. Chem. Int. Ed. 2016, 55, 12845-12848 DOI: 10.1002/anie.201605616
bis(4-nitrophenyl)methanide (in DMSO)	DMSO	N Parameter: 19.92 s_N Parameter: 0.67	ARKIVOC 2008, (x), 37-53 DOI: 10.3998/ark.5550190.0009.a05
beta-(trimethylsilyl)styrene	dichloromethane	N Parameter: -0.43 s_N Parameter: 1.06	Chem. Eur. J. 2014, 20, 1103-1110 DOI: 10.1002/chem.201303215
benzyl isocyanide	dichloromethane	N Parameter: 4.90 s_N Parameter: 0.74	Angew. Chem. Int. Ed. 2007, 46, 3563-3566 DOI: 10.1002/anie.200605205
benzyl (1-phenylvinyl)carbamate	MeCN	N Parameter: 6.21 s_N Parameter: 0.87	Chem. Eur. J. 2012, 18, 5732-5740 DOI: 10.1002/chem.201103519
barbiturate anion (in DMSO)	DMSO	N Parameter: 15.59 s_N Parameter: 0.80	J. Org. Chem. 2017, 82, 8476-8488 DOI: 10.1021/acs.joc.7b01223
azulene	MeCN	N Parameter: 6.66 s_N Parameter: 1.02	Eur. J. Org. Chem. 2009, , 1202-1206 DOI: 10.1002/ejoc.200801099
anisole	dichloromethane	N Parameter: -1.18 s_N Parameter: 1.20	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
anion of triethyl methanetricarboxylate (in DMSO)	DMSO	N Parameter: 15.33 s_N Parameter: 0.72	Eur. J. Org. Chem. 2016, , 1841-1848 DOI: 10.1002/ejoc.201600107
anion of phenylnitromethane (in H2O)	water	N Parameter: 12.05 s_N Parameter: 0.53	J. Org. Chem. 2004, 69, 7565-7576 DOI: 10.1021/jo048773j
anion of phenylnitromethane (in DMSO)	DMSO	N Parameter: 18.29 s_N Parameter: 0.71	J. Org. Chem. 2004, 69, 7565-7576 DOI: 10.1021/jo048773j
anion of phenylnitromethane (in 91M9AN)	MeOH-MeCN mix	N Parameter: 12.51 s_N Parameter: 0.67	Eur. J. Org. Chem. 2006, , 2530-2537 DOI: 10.1002/ejoc.200500769
anion of p-tolylnitromethane (in water)	water	N Parameter: 13.09 s_N Parameter: 0.50	J. Org. Chem. 2004, 69, 7565-7576 DOI: 10.1021/jo048773j
anion of p-tolylnitromethane (in DMSO)	DMSO	N Parameter: 18.31 s_N Parameter: 0.76	J. Org. Chem. 2004, 69, 7565-7576 DOI: 10.1021/jo048773j
anion of p-tolylnitromethane (in 91M9AN)	MeOH-MeCN mix	N Parameter: 13.58 s_N Parameter: 0.64	Eur. J. Org. Chem. 2006, , 2530-2537 DOI: 10.1002/ejoc.200500769
anion of nitromethane (in water)	water	N Parameter: 12.06 s_N Parameter: 0.53	J. Org. Chem. 2004, 69, 7565-7576 DOI: 10.1021/jo048773j
anion of nitromethane (in DMSO)	DMSO	N Parameter: 20.71 s_N Parameter: 0.60	J. Org. Chem. 2004, 69, 7565-7576 DOI: 10.1021/jo048773j
anion of nitromethane (in 91M9AN)	MeOH-MeCN mix	N Parameter: 14.02 s_N Parameter: 0.61	Eur. J. Org. Chem. 2006, , 2530-2537 DOI: 10.1002/ejoc.200500769
anion of nitroethane (in water)	water	N Parameter: 11.25 s_N Parameter: 0.52	J. Org. Chem. 2004, 69, 7565-7576 DOI: 10.1021/jo048773j
anion of nitroethane (in DMSO)	DMSO	N Parameter: 21.54 s_N Parameter: 0.62	J. Org. Chem. 2003, 68, 6880-6886 DOI: 10.1021/jo0344182
anion of nitroethane (in DMF)	DMF	N Parameter: 22.21 s_N Parameter: 0.48	Chem. Eur. J. 2008, 14, 6108-6118 DOI: 10.1002/chem.200800329
anion of nitroethane (in 91M9AN)	MeOH-MeCN mix	N Parameter: 13.41 s_N Parameter: 0.67	Eur. J. Org. Chem. 2006, , 2530-2537 DOI: 10.1002/ejoc.200500769
anion of N,N-diethyl-3-oxo-3-phenylpropanoate (in DMSO)	DMSO	N Parameter: 19.28 s_N Parameter: 0.65	Chem. Eur. J. 2015, 21, 875-884 DOI: 10.1002/chem.201404500
anion of Meldrums acid (in DMSO)	DMSO	N Parameter: 13.91 s_N Parameter: 0.86	Angew. Chem. Int. Ed. 2002, 41, 91-95 DOI: 10.1002/1521-3773(20020104)41:1<91::AID-ANIE91>3.0.CO;2-P
anion of Meldrum's acid (in water)	water	N Parameter: 12.06 s_N Parameter: 0.66	J. Am. Chem. Soc. 2003, 125, 12980-12986 DOI: 10.1021/ja036838e
anion of malononitrile (in water)	water	N Parameter: 19.50 s_N Parameter: 0.55	J. Am. Chem. Soc. 2003, 125, 12980-12986 DOI: 10.1021/ja036838e
anion of malononitrile (in DMSO)	DMSO	N Parameter: 19.36 s_N Parameter: 0.67	Angew. Chem. Int. Ed. 2002, 41, 91-95 DOI: 10.1002/1521-3773(20020104)41:1<91::AID-ANIE91>3.0.CO;2-P
anion of malononitrile (in 91M9AN)	MeOH-MeCN mix	N Parameter: 18.21 s_N Parameter: 0.69	Eur. J. Org. Chem. 2006, , 2530-2537 DOI: 10.1002/ejoc.200500769
anion of ethyl cyanoacetate (in water)	water	N Parameter: 15.57 s_N Parameter: 0.58	J. Am. Chem. Soc. 2003, 125, 12980-12986 DOI: 10.1021/ja036838e
anion of ethyl cyanoacetate (in DMSO)	DMSO	N Parameter: 19.62 s_N Parameter: 0.67	Angew. Chem. Int. Ed. 2002, 41, 91-95 DOI: 10.1002/1521-3773(20020104)41:1<91::AID-ANIE91>3.0.CO;2-P
anion of ethyl cyanoacetate (in 91M9AN)	MeOH-MeCN mix	N Parameter: 18.59 s_N Parameter: 0.65	Eur. J. Org. Chem. 2006, , 2530-2537 DOI: 10.1002/ejoc.200500769
anion of ethyl acetylacetate (in water)	water	N Parameter: 15.99 s_N Parameter: 0.62	J. Am. Chem. Soc. 2003, 125, 12980-12986 DOI: 10.1021/ja036838e
anion of ethyl acetylacetate (in DMSO)	DMSO	N Parameter: 18.82 s_N Parameter: 0.69	Angew. Chem. Int. Ed. 2002, 41, 91-95 DOI: 10.1002/1521-3773(20020104)41:1<91::AID-ANIE91>3.0.CO;2-P
anion of ethyl 3-oxo-3-phenylpropanoate (in DMSO)	DMSO	N Parameter: 17.52 s_N Parameter: 0.74	Chem. Eur. J. 2015, 21, 875-884 DOI: 10.1002/chem.201404500
anion of ethyl 2-nitroacetate (in DMSO)	DMSO	N Parameter: 15.24 s_N Parameter: 0.74	Chem. Eur. J. 2015, 21, 875-884 DOI: 10.1002/chem.201404500
anion of ethyl 2-cyano-2-phenylacetate (in DMSO)	DMSO	N Parameter: 15.85 s_N Parameter: 1.04	Eur. J. Org. Chem. 2017, , 1196-1202 DOI: 10.1002/ejoc.201601513
anion of dimethyl malonate (in 91M9AN)	MeOH-MeCN mix	N Parameter: 18.24 s_N Parameter: 0.64	Eur. J. Org. Chem. 2006, , 2530-2537 DOI: 10.1002/ejoc.200500769
anion of dimedone (in water)	water	N Parameter: 11.77 s_N Parameter: 0.63	J. Am. Chem. Soc. 2003, 125, 12980-12986 DOI: 10.1021/ja036838e
anion of dimedone (in DMSO)	DMSO	N Parameter: 16.27 s_N Parameter: 0.77	Angew. Chem. Int. Ed. 2002, 41, 91-95 DOI: 10.1002/1521-3773(20020104)41:1<91::AID-ANIE91>3.0.CO;2-P
anion of diethyl methylmalonate (in water)	water	N Parameter: 17.68 s_N Parameter: 0.50	J. Am. Chem. Soc. 2003, 125, 12980-12986 DOI: 10.1021/ja036838e
anion of diethyl methylmalonate (in DMSO)	DMSO	N Parameter: 21.13 s_N Parameter: 0.68	J. Am. Chem. Soc. 2003, 125, 12980-12986 DOI: 10.1021/ja036838e
anion of diethyl malonate (in water)	water	N Parameter: 16.15 s_N Parameter: 0.66	J. Am. Chem. Soc. 2003, 125, 12980-12986 DOI: 10.1021/ja036838e
anion of diethyl malonate (in DMSO)	DMSO	N Parameter: 20.22 s_N Parameter: 0.65	Angew. Chem. Int. Ed. 2002, 41, 91-95 DOI: 10.1002/1521-3773(20020104)41:1<91::AID-ANIE91>3.0.CO;2-P
anion of diethyl 2-phenylmalonate (in DMSO)	DMSO	N Parameter: 15.93 s_N Parameter: 0.99	Eur. J. Org. Chem. 2016, , 1841-1848 DOI: 10.1002/ejoc.201600107
anion of diethyl 2-cyclohexylmalonate (in DMSO)	DMSO	N Parameter: 19.23 s_N Parameter: 0.67	Eur. J. Org. Chem. 2016, , 1841-1848 DOI: 10.1002/ejoc.201600107
anion of diethyl 2-butylmalonate (in DMSO)	DMSO	N Parameter: 23.00 s_N Parameter: 0.55	Eur. J. Org. Chem. 2016, , 1841-1848 DOI: 10.1002/ejoc.201600107
anion of diethyl 2-(p-anisyl)malonate (in DMSO)	DMSO	N Parameter: 16.73 s_N Parameter: 0.91	Eur. J. Org. Chem. 2016, , 1841-1848 DOI: 10.1002/ejoc.201600107
anion of diethyl 2-(isopropyl)malonate (in DMSO)	DMSO	N Parameter: 18.74 s_N Parameter: 0.71	Eur. J. Org. Chem. 2016, , 1841-1848 DOI: 10.1002/ejoc.201600107
anion of diethyl 2-(benzoyl)malonate (in DMSO)	DMSO	N Parameter: 13.63 s_N Parameter: 0.80	Eur. J. Org. Chem. 2016, , 1841-1848 DOI: 10.1002/ejoc.201600107
anion of diethyl 2-(acetyl)malonate (in DMSO)	DMSO	N Parameter: 13.83 s_N Parameter: 0.84	Eur. J. Org. Chem. 2016, , 1841-1848 DOI: 10.1002/ejoc.201600107
anion of diethyl 2-(4-nitrophenyl)malonate (in DMSO)	DMSO	N Parameter: 14.94 s_N Parameter: 0.96	Eur. J. Org. Chem. 2016, , 1841-1848 DOI: 10.1002/ejoc.201600107
anion of benzyl trifluoromethyl sulfone (in DMSO)	DMSO	N Parameter: 18.67 s_N Parameter: 0.68	J. Am. Chem. Soc. 2007, 129, 9753-9761 DOI: 10.1021/ja072135b
anion of acetylacetone (in water)	water	N Parameter: 13.73 s_N Parameter: 0.64	J. Am. Chem. Soc. 2003, 125, 12980-12986 DOI: 10.1021/ja036838e
anion of acetylacetone (in DMSO)	DMSO	N Parameter: 17.64 s_N Parameter: 0.73	Angew. Chem. Int. Ed. 2002, 41, 91-95 DOI: 10.1002/1521-3773(20020104)41:1<91::AID-ANIE91>3.0.CO;2-P
anion of 5-phenyl Meldrum's acid (in DMSO)	DMSO	N Parameter: 11.54 s_N Parameter: 0.95	Eur. J. Org. Chem. 2016, , 1841-1848 DOI: 10.1002/ejoc.201600107
anion of 5-(p-anisyl) Meldrum's acid (in DMSO)	DMSO	N Parameter: 12.35 s_N Parameter: 0.90	Eur. J. Org. Chem. 2016, , 1841-1848 DOI: 10.1002/ejoc.201600107
anion of 4-nitrobenzyl-CN (in MeCN)	MeCN	N Parameter: 20.10 s_N Parameter: 0.71	J. Am. Chem. Soc. 2020, 142, 8383-8402 DOI: 10.1021/jacs.0c01960
anion of 4-nitrobenzyl-CN (in DMSO)	DMSO	N Parameter: 19.67 s_N Parameter: 0.68	J. Org. Chem. 2009, 74, 75-81 DOI: 10.1021/jo802241x
anion of 4-nitrobenzyl trifluoromethyl sulfone (in DMSO)	DMSO	N Parameter: 14.49 s_N Parameter: 0.86	J. Am. Chem. Soc. 2007, 129, 9753-9761 DOI: 10.1021/ja072135b
anion of 4-nitrobenzyl trifluoromethyl sulfone (in 91M9AN)	MeOH-MeCN mix	N Parameter: 18.24 s_N Parameter: 0.66	J. Am. Chem. Soc. 2007, 129, 9753-9761 DOI: 10.1021/ja072135b
anion of 4-methylbenzyl trifluoromethyl sulfone (in DMSO)	DMSO	N Parameter: 19.35 s_N Parameter: 0.67	J. Am. Chem. Soc. 2007, 129, 9753-9761 DOI: 10.1021/ja072135b
anion of 4-cyanobenzyl-CN (in DMSO)	DMSO	N Parameter: 25.11 s_N Parameter: 0.54	J. Org. Chem. 2009, 74, 75-81 DOI: 10.1021/jo802241x
anion of 4-cyanobenzyl trifluoromethyl sulfone (in MeCN)	MeCN	N Parameter: 15.62 s_N Parameter: 0.99	J. Am. Chem. Soc. 2020, 142, 8383-8402 DOI: 10.1021/jacs.0c01960
anion of 4-cyanobenzyl trifluoromethyl sulfone (in DMSO)	DMSO	N Parameter: 16.28 s_N Parameter: 0.75	J. Am. Chem. Soc. 2007, 129, 9753-9761 DOI: 10.1021/ja072135b
anion of 4-cyanobenzyl trifluoromethyl sulfone (in 91M9AN)	MeOH-MeCN mix	N Parameter: 19.49 s_N Parameter: 0.63	J. Am. Chem. Soc. 2007, 129, 9753-9761 DOI: 10.1021/ja072135b
anion of 4-(trifluoromethyl)benzyl-CN (in DMSO)	DMSO	N Parameter: 27.28 s_N Parameter: 0.50	J. Org. Chem. 2009, 74, 75-81 DOI: 10.1021/jo802241x
anion of 4-(trifluoromethyl)benzyl trifluoromethyl sulfone (in MeCN)	MeCN	N Parameter: 16.15 s_N Parameter: 0.99	J. Am. Chem. Soc. 2020, 142, 8383-8402 DOI: 10.1021/jacs.0c01960
anion of 4-(trifluoromethyl)benzyl trifluoromethyl sulfone (in DMSO)	DMSO	N Parameter: 17.33 s_N Parameter: 0.74	J. Am. Chem. Soc. 2007, 129, 9753-9761 DOI: 10.1021/ja072135b
anion of 4-(trifluoromethyl)benzyl trifluoromethyl sulfone (in 91M9AN)	MeOH-MeCN mix	N Parameter: 20.72 s_N Parameter: 0.58	J. Am. Chem. Soc. 2007, 129, 9753-9761 DOI: 10.1021/ja072135b
anion of 3-oxo-3-phenylpropanenitrile (in DMSO)	DMSO	N Parameter: 16.55 s_N Parameter: 0.78	Chem. Eur. J. 2015, 21, 875-884 DOI: 10.1002/chem.201404500
anion of 3-methyl acetylacetone (in water)	water	N Parameter: 14.33 s_N Parameter: 0.69	J. Am. Chem. Soc. 2003, 125, 12980-12986 DOI: 10.1021/ja036838e
anion of 3-methyl acetylacetone (in DMSO)	DMSO	N Parameter: 18.38 s_N Parameter: 0.72	J. Am. Chem. Soc. 2003, 125, 12980-12986 DOI: 10.1021/ja036838e
anion of 2-phenylmalononitrile (in DMSO)	DMSO	N Parameter: 15.58 s_N Parameter: 1.00	Eur. J. Org. Chem. 2017, , 1196-1202 DOI: 10.1002/ejoc.201601513
anion of 2-phenyl-propionitrile (in DMSO)	DMSO	N Parameter: 28.95 s_N Parameter: 0.58	J. Org. Chem. 2009, 74, 75-81 DOI: 10.1021/jo802241x
anion of 2-phenyl-2-(phenylsulfonyl)acetonitrile (in DMSO)	DMSO	N Parameter: 15.97 s_N Parameter: 0.72	Eur. J. Org. Chem. 2017, , 1196-1202 DOI: 10.1002/ejoc.201601513
anion of 2-nitropropane (in water)	water	N Parameter: 10.69 s_N Parameter: 0.56	J. Org. Chem. 2004, 69, 7565-7576 DOI: 10.1021/jo048773j
anion of 2-nitropropane (in DMSO)	DMSO	N Parameter: 20.61 s_N Parameter: 0.69	J. Org. Chem. 2004, 69, 7565-7576 DOI: 10.1021/jo048773j
anion of 2-nitropropane (in 91M9AN)	MeOH-MeCN mix	N Parameter: 12.20 s_N Parameter: 0.71	Eur. J. Org. Chem. 2006, , 2530-2537 DOI: 10.1002/ejoc.200500769
anion of 2-nitro-1-phenylethan-1-one (in DMSO)	DMSO	N Parameter: 13.91 s_N Parameter: 0.76	Chem. Eur. J. 2015, 21, 875-884 DOI: 10.1002/chem.201404500
anion of 2-(4-NO2-C6H4)propionitrile (in DMSO)	DMSO	N Parameter: 19.61 s_N Parameter: 0.60	J. Org. Chem. 2009, 74, 75-81 DOI: 10.1021/jo802241x
anion of 2-(4-CN-C6H4)propionitrile (in DMSO)	DMSO	N Parameter: 25.35 s_N Parameter: 0.56	J. Org. Chem. 2009, 74, 75-81 DOI: 10.1021/jo802241x
anion of 1-phenylpropan-2-one (in DMSO)	DMSO	N Parameter: 24.99 s_N Parameter: 0.60	Chem. Eur. J. 2015, 21, 875-884 DOI: 10.1002/chem.201404500
anion of 1-phenylbutane-1,3-dione (in DMSO)	DMSO	N Parameter: 16.03 s_N Parameter: 0.86	Chem. Eur. J. 2015, 21, 875-884 DOI: 10.1002/chem.201404500
anion of 1-phenyl-2-(phenylsulfonyl)ethanone (in DMSO)	DMSO	N Parameter: 17.19 s_N Parameter: 0.56	Chem. Eur. J. 2015, 21, 875-884 DOI: 10.1002/chem.201404500
anion of 1,3-diphenylpropane-1,3-dione (in DMSO)	DMSO	N Parameter: 17.46 s_N Parameter: 0.65	Chem. Eur. J. 2015, 21, 875-884 DOI: 10.1002/chem.201404500
anion of 1,2-diphenylethanone (in DMSO)	DMSO	N Parameter: 23.15 s_N Parameter: 0.60	Chem. Eur. J. 2015, 21, 875-884 DOI: 10.1002/chem.201404500
anion of 1,2,3-triphenylpropane-1,3-dione (in DMSO)	DMSO	N Parameter: 14.99 s_N Parameter: 0.83	Eur. J. Org. Chem. 2017, , 1196-1202 DOI: 10.1002/ejoc.201601513
anion of (phenylmethylenedisulfonyl)dibenzene (in DMSO)	DMSO	N Parameter: 15.07 s_N Parameter: 0.79	Eur. J. Org. Chem. 2017, , 1196-1202 DOI: 10.1002/ejoc.201601513
anion of (benzylsulfonyl)benzene (in DMSO)	DMSO	N Parameter: 25.77 s_N Parameter: 0.56	Chem. Eur. J. 2015, 21, 875-884 DOI: 10.1002/chem.201404500
anion of (4-NO2-C6H4)CH2SO2Ph (in MeCN)	MeCN	N Parameter: 19.90 s_N Parameter: 0.66	J. Am. Chem. Soc. 2020, 142, 8383-8402 DOI: 10.1021/jacs.0c01960
anion of (4-NO2-C6H4)CH2SO2Ph (in DMSO)	DMSO	N Parameter: 18.50 s_N Parameter: 0.75	Org. Biomol. Chem. 2008, 6, 3052-3058 DOI: 10.1039/b805604h
anion of (4-nitrophenyl)nitromethane (in water)	water	N Parameter: 13.58 s_N Parameter: 0.52	J. Org. Chem. 2004, 69, 7565-7576 DOI: 10.1021/jo048773j
anion of (4-nitrophenyl)nitromethane (in DMSO)	DMSO	N Parameter: 16.29 s_N Parameter: 0.75	J. Org. Chem. 2004, 69, 7565-7576 DOI: 10.1021/jo048773j
anion of (4-nitrophenyl)nitromethane (in 91M9AN)	MeOH-MeCN mix	N Parameter: 14.05 s_N Parameter: 0.72	Eur. J. Org. Chem. 2006, , 2530-2537 DOI: 10.1002/ejoc.200500769
anion of (4-cyanophenyl)nitromethane (in water)	water	N Parameter: 13.23 s_N Parameter: 0.52	J. Org. Chem. 2004, 69, 7565-7576 DOI: 10.1021/jo048773j
anion of (4-cyanophenyl)nitromethane (in DMSO)	DMSO	N Parameter: 16.96 s_N Parameter: 0.73	J. Org. Chem. 2004, 69, 7565-7576 DOI: 10.1021/jo048773j
anion of (4-cyanophenyl)nitromethane (in 91M9AN)	MeOH-MeCN mix	N Parameter: 13.92 s_N Parameter: 0.74	Eur. J. Org. Chem. 2006, , 2530-2537 DOI: 10.1002/ejoc.200500769
anion of (4-CN-C6H4)CH2SO2Ph (in DMSO)	DMSO	N Parameter: 22.60 s_N Parameter: 0.57	Org. Biomol. Chem. 2008, 6, 3052-3058 DOI: 10.1039/b805604h
anion of (4-CF3-C6H4)CH2SO2Ph (in DMSO)	DMSO	N Parameter: 24.30 s_N Parameter: 0.51	Org. Biomol. Chem. 2008, 6, 3052-3058 DOI: 10.1039/b805604h
anion of (3-nitrophenyl)nitromethane (in water)	water	N Parameter: 14.25 s_N Parameter: 0.46	J. Org. Chem. 2004, 69, 7565-7576 DOI: 10.1021/jo048773j
anion of (3-nitrophenyl)nitromethane (in DMSO)	DMSO	N Parameter: 18.06 s_N Parameter: 0.71	J. Org. Chem. 2004, 69, 7565-7576 DOI: 10.1021/jo048773j
anion of (3-nitrophenyl)nitromethane (in 91M9AN)	MeOH-MeCN mix	N Parameter: 14.75 s_N Parameter: 0.71	Eur. J. Org. Chem. 2006, , 2530-2537 DOI: 10.1002/ejoc.200500769
alpha-methylstyrene	dichloromethane	N Parameter: 2.35 s_N Parameter: 1.00	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
alpha-(trimethylsilyl)styrene	dichloromethane	N Parameter: -1.13 s_N Parameter: 1.46	Chem. Eur. J. 2014, 20, 1103-1110 DOI: 10.1002/chem.201303215
alpha-(pentamethyldisilyl)styrene	dichloromethane	N Parameter: 0.61 s_N Parameter: 1.01	Chem. Eur. J. 2014, 20, 1103-1110 DOI: 10.1002/chem.201303215
alpha-(N-piperidino)styrene (in MeCN)	MeCN	N Parameter: 11.60 s_N Parameter: 0.80	Chem. Eur. J. 2018, 24, 5901-5910 DOI: 10.1002/chem.201705962
alpha-(N-morpholino)styrene (in MeCN)	MeCN	N Parameter: 10.30 s_N Parameter: 0.80	Chem. Eur. J. 2018, 24, 5901-5910 DOI: 10.1002/chem.201705962
alpha-(N-morpholino)styrene	dichloromethane	N Parameter: 9.96 s_N Parameter: 0.79	Chem. Eur. J. 2003, 9, 2209-2218 DOI: 10.1002/chem.200204666
allyltris(trimethylsilyl)silane	dichloromethane	N Parameter: 1.95 s_N Parameter: 0.98	Org. Lett. 2010, 12, 5206-5209 DOI: 10.1021/ol102220e
allyltriphenylstannane	dichloromethane	N Parameter: 3.09 s_N Parameter: 0.90	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
allyltriphenylsilane	dichloromethane	N Parameter: -0.13 s_N Parameter: 1.21	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
allyltriphenylgermane	dichloromethane	N Parameter: 1.20 s_N Parameter: 0.90	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
allyltrimethylsilane	dichloromethane	N Parameter: 1.68 s_N Parameter: 1.00	J. Am. Chem. Soc. 2012, 134, 13902-13911 DOI: 10.1021/ja306522b
allyltriisopropylsilane	dichloromethane	N Parameter: 2.04 s_N Parameter: 0.95	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
allyltrihexylsilane	dichloromethane	N Parameter: 2.11 s_N Parameter: 0.95	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
allyltriethylsilane	dichloromethane	N Parameter: 1.93 s_N Parameter: 0.95	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
allyltributylstannane	dichloromethane	N Parameter: 5.46 s_N Parameter: 0.89	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
allyltri-n-butylsilane	dichloromethane	N Parameter: 2.09 s_N Parameter: 0.95	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
allylchlorodimethylsilane	dichloromethane	N Parameter: -0.57 s_N Parameter: 1.06	J. Am. Chem. Soc. 2012, 134, 13902-13911 DOI: 10.1021/ja306522b
allyl-tert.butyl-dimethylsilane	dichloromethane	N Parameter: 1.80 s_N Parameter: 0.95	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
7-azaindole	MeCN	N Parameter: 3.87 s_N Parameter: 1.10	J. Org. Chem. 2006, 71, 9088-9095 DOI: 10.1021/jo0614339
6-methyl-3-(phenyl-l3-iodanylidene)dihydro-2H-pyran-2,4(3H)-dione (in CH2Cl2)	dichloromethane	N Parameter: 4.67 s_N Parameter: 0.92	J. Am. Chem. Soc. 2016, 138, 10304-10313 DOI: 10.1021/jacs.6b05768
6-(julolidin-9-yl)fulvene	MeCN	N Parameter: 7.79 s_N Parameter: 1.06	Eur. J. Org. Chem. 2009, , 1202-1206 DOI: 10.1002/ejoc.200801099
6-(4-dimethylamino-phenyl)fulvene	MeCN	N Parameter: 6.72 s_N Parameter: 0.87	Eur. J. Org. Chem. 2009, , 1202-1206 DOI: 10.1002/ejoc.200801099
6,6-dimethylfulvene	MeCN	N Parameter: 3.93 s_N Parameter: 0.88	Eur. J. Org. Chem. 2009, , 1202-1206 DOI: 10.1002/ejoc.200801099
5-methyl-indole	MeCN	N Parameter: 6.00 s_N Parameter: 1.10	J. Org. Chem. 2006, 71, 9088-9095 DOI: 10.1021/jo0614339
5-methoxy-indole	dichloromethane	N Parameter: 6.22 s_N Parameter: 1.12	J. Org. Chem. 2006, 71, 9088-9095 DOI: 10.1021/jo0614339
5-methoxy-2-methylindole	MeCN	N Parameter: 7.26 s_N Parameter: 1.10	J. Org. Chem. 2006, 71, 9088-9095 DOI: 10.1021/jo0614339
5-hydroxy-indole	MeCN	N Parameter: 6.44 s_N Parameter: 1.10	J. Org. Chem. 2006, 71, 9088-9095 DOI: 10.1021/jo0614339
5-cyano-indole	MeCN	N Parameter: 2.83 s_N Parameter: 1.10	J. Org. Chem. 2006, 71, 9088-9095 DOI: 10.1021/jo0614339
5-chloro-indole	MeCN	N Parameter: 4.42 s_N Parameter: 1.10	J. Org. Chem. 2006, 71, 9088-9095 DOI: 10.1021/jo0614339
5-chloro-2-methylindole	MeCN	N Parameter: 6.08 s_N Parameter: 1.10	J. Org. Chem. 2006, 71, 9088-9095 DOI: 10.1021/jo0614339
5-bromo-indole	MeCN	N Parameter: 4.38 s_N Parameter: 1.10	J. Org. Chem. 2006, 71, 9088-9095 DOI: 10.1021/jo0614339
5-benzyl-2,2-dimethyl-4,6-dioxo-1,3-dioxan-5-ide (in DMSO)	DMSO	N Parameter: 15.02 s_N Parameter: 0.75	Chem. Eur. J. 2014, 20, 11069-11077 DOI: 10.1002/chem.201403161
5-amino-indole	MeCN	N Parameter: 7.22 s_N Parameter: 1.10	J. Org. Chem. 2006, 71, 9088-9095 DOI: 10.1021/jo0614339
5-(tris(pentafluorophenyl)siloxy)-2,3-dihydrofuran	dichloromethane	N Parameter: 8.16 s_N Parameter: 0.67	Eur. J. Org. Chem. 2005, , 1760-1764 DOI: 10.1002/ejoc.200400706
5-(triphenylsiloxy)-2,3-dihydrofuran	dichloromethane	N Parameter: 11.28 s_N Parameter: 0.91	Eur. J. Org. Chem. 2005, , 1760-1764 DOI: 10.1002/ejoc.200400706
5-(trimethylsiloxy)-2,3-dihydrofuran (in MeCN)	MeCN	N Parameter: 12.34 s_N Parameter: 0.72	J. Am. Chem. Soc. 2013, 135, 6579-6587 DOI: 10.1021/ja401106x
5-(trimethylsiloxy)-2,3-dihydrofuran	dichloromethane	N Parameter: 12.56 s_N Parameter: 0.70	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
5-(tert-Butyl)-1,3-diisopropyl-4-methylene-4,5-dihydro-1H-1,2,3-triazol-3-ium-5-ide (in THF)	THF	N Parameter: 31.92 s_N Parameter: 0.52	Angew. Chem. Int. Ed. 2023, 62, e202309790 DOI: 10.1002/anie.202309790
5-(4-cyanobenzyl)-2,2-dimethyl-4,6-dioxo-1,3-dioxan-5-ide (in DMSO)	DMSO	N Parameter: 13.79 s_N Parameter: 0.86	Chem. Eur. J. 2014, 20, 11069-11077 DOI: 10.1002/chem.201403161
5-(4-(methoxy)benzyl)-2,2-dimethyl-4,6-dioxo-1,3-dioxan-5-ide (in DMSO)	DMSO	N Parameter: 15.13 s_N Parameter: 0.75	Chem. Eur. J. 2014, 20, 11069-11077 DOI: 10.1002/chem.201403161
5-(4-(dimethylamino)benzyl)-2,2-dimethyl-4,6-dioxo-1,3-dioxan-5-ide (in DMSO)	DMSO	N Parameter: 14.48 s_N Parameter: 0.86	Chem. Eur. J. 2014, 20, 11069-11077 DOI: 10.1002/chem.201403161
4-methyl-penta-1,3-diene	dichloromethane	N Parameter: 2.60 s_N Parameter: 1.00	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
4-methyl-N-(2-phenylethynyl)-N-(phenylmethyl)benzenesulfonamide	dichloromethane	N Parameter: 3.85 s_N Parameter: 0.84	Angew. Chem. Int. Ed. 2014, 53, 4968-4971 DOI: 10.1002/anie.201402055
4-methyl-5-(trimethylsiloxy)-2,3-dihydrofuran	dichloromethane	N Parameter: 11.50 s_N Parameter: 0.91	Eur. J. Org. Chem. 2004, , 2791-2796 DOI: 10.1002/ejoc.200400134
4-methoxy-indole	MeCN	N Parameter: 5.41 s_N Parameter: 1.10	J. Org. Chem. 2006, 71, 9088-9095 DOI: 10.1021/jo0614339
4-cyanophenyl isocyanide	dichloromethane	N Parameter: 3.57 s_N Parameter: 0.72	Angew. Chem. Int. Ed. 2007, 46, 3563-3566 DOI: 10.1002/anie.200605205
4-(trimethylsilyl)but-1-en-3-ynyl-Co2(CO)6	dichloromethane	N Parameter: -1.11 s_N Parameter: 0.92	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
4-(trimethylsilyl)but-1-en-3-ynyl-Co2(CO)5(PPh3)	dichloromethane	N Parameter: -0.76 s_N Parameter: 0.90	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
4-(bis(trimethylsiloxy)amino)pent-4-enoic acid methyl ester	dichloromethane	N Parameter: 3.84 s_N Parameter: 0.87	J. Org. Chem. 2001, 66, 3196-3200 DOI: 10.1021/jo0015927
4,4,5,5-tetramethyl-2-prop-2-enyl-1,3,2-dioxaborolane (in CH2Cl2)	dichloromethane	N Parameter: -0.64 s_N Parameter: 1.10	J. Am. Chem. Soc. 2017, 139, 15324-15327 DOI: 10.1021/jacs.7b10240
3-pyrrolidino-1H-indene (in MeCN)	MeCN	N Parameter: 15.27 s_N Parameter: 0.93	Synthesis 2019, 51, 1157-1170 DOI: 10.1055/s-0037-1611634
3-methylanisole	dichloromethane	N Parameter: 0.13 s_N Parameter: 1.27	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
3-methyl-2-(trimethylsiloxy)but-1-ene	dichloromethane	N Parameter: 5.41 s_N Parameter: 0.90	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
3-methyl-2,4-dioxotetrahydro-2H-pyran-3-ide (in DMSO)	DMSO	N Parameter: 14.46 s_N Parameter: 0.91	Eur. J. Org. Chem. 2015, , 7594-7601 DOI: 10.1002/ejoc.201501107
3-methoxythiophene	MeCN	N Parameter: 3.06 s_N Parameter: 1.19	J. Am. Chem. Soc. 2013, 135, 6317-6324 DOI: 10.1021/ja4017655
3-mesityl-1-methyl-1H-imidazol-3-ium-2-ide (in THF)	THF	N Parameter: 21.50 s_N Parameter: 0.45	Org. Lett. 2016, 18, 3566-3569 DOI: 10.1021/acs.orglett.6b01525
3-ethyl-2,4-dimethylpyrrole	MeCN	N Parameter: 11.63 s_N Parameter: 0.95	Eur. J. Org. Chem. 2008, , 2369-2374 DOI: 10.1002/ejoc.200800092
3-diazoindolin-2-one	dichloromethane	N Parameter: 3.16 s_N Parameter: 1.03	Eur. J. Org. Chem. 2023, 26, e202300005 DOI: 10.1002/ejoc.202300005
3-acetyl-2-oxotetrahydro-2H-pyran-3-ide (in DMSO)	DMSO	N Parameter: 17.00 s_N Parameter: 0.74	Eur. J. Org. Chem. 2015, , 7594-7601 DOI: 10.1002/ejoc.201501107
3-(trimethylsilyl)cyclopentene	dichloromethane	N Parameter: 1.77 s_N Parameter: 1.10	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
3-(trimethylsiloxy)-1H-indene (in MeCN)	MeCN	N Parameter: 7.32 s_N Parameter: 0.82	Synthesis 2019, 51, 1157-1170 DOI: 10.1055/s-0037-1611634
3-(trihexylsilyl)cyclopentene	dichloromethane	N Parameter: 1.98 s_N Parameter: 1.10	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
3-(tert-butyl)-1-methyl-1H-imidazol-3-ium-2-ide (in THF)	THF	N Parameter: 16.54 s_N Parameter: 0.47	Org. Lett. 2016, 18, 3566-3569 DOI: 10.1021/acs.orglett.6b01525
3-(4-methoxyphenyl)-1-methyl-1H-imidazol-3-ium-2-ide (in THF)	THF	N Parameter: 20.41 s_N Parameter: 0.46	Org. Lett. 2016, 18, 3566-3569 DOI: 10.1021/acs.orglett.6b01525
3-(2,6-dimethoxyphenyl)-1-methyl-1H-imidazol-3-ium-2-ide (in THF)	THF	N Parameter: 23.00 s_N Parameter: 0.46	Org. Lett. 2016, 18, 3566-3569 DOI: 10.1021/acs.orglett.6b01525
3,3-dimethyl-2-(trimethylsiloxy)buten	dichloromethane	N Parameter: 3.78 s_N Parameter: 0.79	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
3,3,3-trifluoro-2-(trimethylsiloxy)propene	dichloromethane	N Parameter: -2.94 s_N Parameter: 1.11	Org. Lett. 2012, 14, 3990-3993 DOI: 10.1021/ol301766w
2H-benzo[d][1,3]dithiol-2-ide 1,1,3,3-tetraoxide (in DMSO)	DMSO	N Parameter: 16.06 s_N Parameter: 0.69	Angew. Chem. Int. Ed. 2016, 55, 12845-12848 DOI: 10.1002/anie.201605616
2-thiobarbiturate anion (in DMSO)	DMSO	N Parameter: 14.24 s_N Parameter: 0.82	J. Org. Chem. 2017, 82, 8476-8488 DOI: 10.1021/acs.joc.7b01223
2-phenyl-allyltrimethylsilane	dichloromethane	N Parameter: 5.38 s_N Parameter: 0.89	Chem. Eur. J. 2014, 20, 1103-1110 DOI: 10.1002/chem.201303215
2-phenyl-4-(trimethylsilyl)but-1-en-3-ynyl-Co2(CO)6	dichloromethane	N Parameter: 1.33 s_N Parameter: 0.90	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
2-PhCH(-)CO2Et (in DMSO)	DMSO	N Parameter: 27.54 s_N Parameter: 0.57	Eur. J. Org. Chem. 2013, , 4255-4261 DOI: 10.1002/ejoc.201300265
2-oxo-2-phenyl-1-(quinolin-1-ium-1-yl)ethan-1-ide (in DMSO)	DMSO	N Parameter: 19.38 s_N Parameter: 0.50	J. Am. Chem. Soc. 2013, 135, 15216-15224 DOI: 10.1021/ja407885h
2-oxo-2-phenyl-1-(pyridin-1-ium-1-yl)ethan-1-ide (in DMSO)	DMSO	N Parameter: 19.46 s_N Parameter: 0.58	J. Am. Chem. Soc. 2013, 135, 15216-15224 DOI: 10.1021/ja407885h
2-oxo-1-(pyridin-1-ium-1-yl)propan-1-ide (in DMSO)	DMSO	N Parameter: 20.24 s_N Parameter: 0.60	J. Am. Chem. Soc. 2013, 135, 15216-15224 DOI: 10.1021/ja407885h
2-methylthiophene	dichloromethane	N Parameter: 1.35 s_N Parameter: 0.99	J. Am. Chem. Soc. 2012, 134, 13902-13911 DOI: 10.1021/ja306522b
2-methylpropene (isobutylene)	dichloromethane	N Parameter: 1.11 s_N Parameter: 0.98	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
2-methylindole	MeCN	N Parameter: 6.91 s_N Parameter: 1.10	J. Org. Chem. 2006, 71, 9088-9095 DOI: 10.1021/jo0614339
2-methylfuran	dichloromethane	N Parameter: 3.61 s_N Parameter: 1.11	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
2-methyl-pent-1-ene	dichloromethane	N Parameter: 0.84 s_N Parameter: 1.06	J. Am. Chem. Soc. 2012, 134, 13902-13911 DOI: 10.1021/ja306522b
2-methyl-buta-1,3-diene (isoprene)	dichloromethane	N Parameter: 1.10 s_N Parameter: 0.98	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
2-methyl-but-2-ene	dichloromethane	N Parameter: 0.65 s_N Parameter: 1.17	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
2-methyl-but-1-ene	dichloromethane	N Parameter: 1.00 s_N Parameter: 1.00	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
2-methyl-1-(trimethylsiloxy)propen	dichloromethane	N Parameter: 3.94 s_N Parameter: 1.00	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
2-methoxy-2H-benzo[d][1,3]dithiol-2-ide 1,1,3,3-tetraoxide (in DMSO)	DMSO	N Parameter: 17.36 s_N Parameter: 0.71	Angew. Chem. Int. Ed. 2016, 55, 12845-12848 DOI: 10.1002/anie.201605616
2-fluoro-2H-benzo[d][1,3]dithiol-2-ide 1,1,3,3-tetraoxide (in DMSO)	DMSO	N Parameter: 19.03 s_N Parameter: 0.58	Angew. Chem. Int. Ed. 2016, 55, 12845-12848 DOI: 10.1002/anie.201605616
2-ethoxy-2-oxo-1-(pyridin-1-ium-1-yl)ethan-1-ide (in DMSO)	DMSO	N Parameter: 26.71 s_N Parameter: 0.37	J. Am. Chem. Soc. 2013, 135, 15216-15224 DOI: 10.1021/ja407885h
2-ethoxy-2-oxo-1-(phenylsulfonyl)ethan-1-ide (in DMSO)	DMSO	N Parameter: 18.81 s_N Parameter: 0.59	Angew. Chem. Int. Ed. 2016, 55, 12845-12848 DOI: 10.1002/anie.201605616
2-ethoxy-1-methoxy-2-oxo-1-(phenylsulfonyl)ethan-1-ide (in DMSO)	DMSO	N Parameter: 19.15 s_N Parameter: 0.59	Angew. Chem. Int. Ed. 2016, 55, 12845-12848 DOI: 10.1002/anie.201605616
2-ethoxy-1-fluoro-2-oxo-1-(phenylsulfonyl)ethan-1-ide (in DMSO)	DMSO	N Parameter: 20.51 s_N Parameter: 0.64	Angew. Chem. Int. Ed. 2016, 55, 12845-12848 DOI: 10.1002/anie.201605616
2-diazoindandione	dichloromethane	N Parameter: 0.16 s_N Parameter: 0.86	Eur. J. Org. Chem. 2023, 26, e202300005 DOI: 10.1002/ejoc.202300005
2-diazoindan-1-one	dichloromethane	N Parameter: 5.61 s_N Parameter: 0.65	Eur. J. Org. Chem. 2023, 26, e202300005 DOI: 10.1002/ejoc.202300005
2-diazocyclohexanone	dichloromethane	N Parameter: 3.44 s_N Parameter: 0.83	Eur. J. Org. Chem. 2023, 26, e202300005 DOI: 10.1002/ejoc.202300005
2-diazobenzothiophen-3(2H)-one	dichloromethane	N Parameter: 0.40 s_N Parameter: 0.93	Eur. J. Org. Chem. 2023, 26, e202300005 DOI: 10.1002/ejoc.202300005
2-diazo-1-tetralone	dichloromethane	N Parameter: 3.51 s_N Parameter: 0.86	Eur. J. Org. Chem. 2023, 26, e202300005 DOI: 10.1002/ejoc.202300005
2-diazo-1-benzosuberone	dichloromethane	N Parameter: 2.72 s_N Parameter: 0.96	Eur. J. Org. Chem. 2023, 26, e202300005 DOI: 10.1002/ejoc.202300005
2-cyclopropylpropene	dichloromethane	N Parameter: 2.60 s_N Parameter: 1.00	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
2-chloropropene	dichloromethane	N Parameter: -3.65 s_N Parameter: 1.97	J. Am. Chem. Soc. 2012, 134, 13902-13911 DOI: 10.1021/ja306522b
2-chloro-1,3-diethoxy-1,3-dioxopropan-2-ide (in DMSO)	DMSO	N Parameter: 18.19 s_N Parameter: 0.74	Angew. Chem. Int. Ed. 2016, 55, 12845-12848 DOI: 10.1002/anie.201605616
2-(tris(trimethylsilyl)silyl)propene	dichloromethane	N Parameter: -0.31 s_N Parameter: 0.99	Chem. Eur. J. 2014, 20, 1103-1110 DOI: 10.1002/chem.201303215
2-(tris(trimethylsilyl)siloxy)propene	dichloromethane	N Parameter: 6.04 s_N Parameter: 0.82	Org. Lett. 2010, 12, 5206-5209 DOI: 10.1021/ol102220e
2-(tris(pentafluorophenyl)siloxy)-propene	dichloromethane	N Parameter: 0.58 s_N Parameter: 0.91	Eur. J. Org. Chem. 2005, , 1760-1764 DOI: 10.1002/ejoc.200400706
2-(triphenylsiloxy)propene	dichloromethane	N Parameter: 4.46 s_N Parameter: 0.90	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
2-(trimethylsilyl)thiophene	dichloromethane	N Parameter: -0.80 s_N Parameter: 1.00	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
2-(trimethylsilyl)propene	dichloromethane	N Parameter: -1.46 s_N Parameter: 1.05	Chem. Eur. J. 2014, 20, 1103-1110 DOI: 10.1002/chem.201303215
2-(trimethylsilyl)furan	dichloromethane	N Parameter: 2.16 s_N Parameter: 1.10	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
2-(trimethylsiloxy)propene	dichloromethane	N Parameter: 5.41 s_N Parameter: 0.91	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
2-(trimethylsiloxy)furan	dichloromethane	N Parameter: 7.22 s_N Parameter: 1.00	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
2-(trimethylsiloxy)buta-1,3-diene	dichloromethane	N Parameter: 4.83 s_N Parameter: 0.90	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
2-(trimethylsiloxy)-5,6-dihydro-4H-pyran (in MeCN)	MeCN	N Parameter: 10.52 s_N Parameter: 0.78	J. Am. Chem. Soc. 2013, 135, 6579-6587 DOI: 10.1021/ja401106x
2-(trimethylsiloxy)-5,6-dihydro-4H-pyran	dichloromethane	N Parameter: 10.61 s_N Parameter: 0.86	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
2-(triisopropylsiloxy)propene	dichloromethane	N Parameter: 5.38 s_N Parameter: 0.85	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
2-(triethylsilyl)furan	dichloromethane	N Parameter: 2.20 s_N Parameter: 1.10	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
2-(tributylstannyl)thiophene	dichloromethane	N Parameter: 1.53 s_N Parameter: 1.00	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
2-(tributylstannyl)furan	dichloromethane	N Parameter: 3.63 s_N Parameter: 1.10	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
2-(tributylsilyl)furan	dichloromethane	N Parameter: 2.37 s_N Parameter: 1.10	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
2-(tert.butyldimethylsiloxy)propene	dichloromethane	N Parameter: 5.58 s_N Parameter: 0.90	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
2-(tert-butoxy)-1-((diphenylmethylene)amino)-2-oxoethan-1-ide (in DMSO)	DMSO	N Parameter: 27.77 s_N Parameter: 0.47	Tetrahedron 2019, 75, 459-463 DOI: 10.1016/j.tet.2018.11.075
2-(pyrid-4-yl)CH(-)CO2Et (in DMSO)	DMSO	N Parameter: 23.27 s_N Parameter: 0.70	Eur. J. Org. Chem. 2013, , 4255-4261 DOI: 10.1002/ejoc.201300265
2-(pentamethyldisilyl)propene	dichloromethane	N Parameter: -0.26 s_N Parameter: 0.95	Chem. Eur. J. 2014, 20, 1103-1110 DOI: 10.1002/chem.201303215
2-(diethylamino)-2-oxo-1-(pyridin-1-ium-1-yl)ethan-1-ide (in DMSO)	DMSO	N Parameter: 27.45 s_N Parameter: 0.38	J. Am. Chem. Soc. 2013, 135, 15216-15224 DOI: 10.1021/ja407885h
2-(bis(trimethylsiloxy)amino)propene	dichloromethane	N Parameter: 4.76 s_N Parameter: 0.86	J. Org. Chem. 2001, 66, 3196-3200 DOI: 10.1021/jo0015927
2-(bis(tert-butyldimethylsiloxy)amino)propene	dichloromethane	N Parameter: 4.23 s_N Parameter: 0.93	J. Org. Chem. 2001, 66, 3196-3200 DOI: 10.1021/jo0015927
2-(benzylideneamino)-1-ethoxy-1-oxopropan-2-ide (in DMSO)	DMSO	N Parameter: 30.82 s_N Parameter: 0.41	Tetrahedron 2019, 75, 459-463 DOI: 10.1016/j.tet.2018.11.075
2-(4-NO2-C6H4)CH(-)CO2Et (in DMSO)	DMSO	N Parameter: 20.00 s_N Parameter: 0.71	Eur. J. Org. Chem. 2013, , 4255-4261 DOI: 10.1002/ejoc.201300265
2-(4-CN-C6H4)CH(-)CO2Et (in DMSO)	DMSO	N Parameter: 23.64 s_N Parameter: 0.65	Eur. J. Org. Chem. 2013, , 4255-4261 DOI: 10.1002/ejoc.201300265
2-(4-Br-C6H4)CH(-)CO2Et (in DMSO)	DMSO	N Parameter: 27.62 s_N Parameter: 0.53	Eur. J. Org. Chem. 2013, , 4255-4261 DOI: 10.1002/ejoc.201300265
2-(3-Cl-C6H4)CH(-)CO2Et (in DMSO)	DMSO	N Parameter: 27.57 s_N Parameter: 0.53	Eur. J. Org. Chem. 2013, , 4255-4261 DOI: 10.1002/ejoc.201300265
2-((2,2,5,5-tetramethyl-1-styryl-2,5-dihydro-1H-imidazol-4-yl)thio)acetonitrile (in MeCN)	MeCN	N Parameter: 7.74 s_N Parameter: 0.87	Chem. Commun. 2023, 59, 8091-8084 DOI: 10.1039/d3cc01912h
2-((2,2,5,5-tetramethyl-1-styryl-2,5-dihydro-1H-imidazol-4-yl)thio)acetonitrile (in CH2Cl2)	dichloromethane	N Parameter: 7.06 s_N Parameter: 1.11	Chem. Commun. 2023, 59, 8091-8084 DOI: 10.1039/d3cc01912h
2-((2,2,5,5-tetramethyl-1-(prop-1-en-1-yl)-2,5-dihydro-1H-imidazol-4-yl)thio)acetonitrile (in MeCN)	MeCN	N Parameter: 9.25 s_N Parameter: 0.84	Chem. Commun. 2023, 59, 8091-8084 DOI: 10.1039/d3cc01912h
2,7-dimethylocta-1,7-diene	dichloromethane	N Parameter: 1.58 s_N Parameter: 1.00	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
2,6-dimethylphenyl isocyanide	dichloromethane	N Parameter: 4.59 s_N Parameter: 0.87	Angew. Chem. Int. Ed. 2007, 46, 3563-3566 DOI: 10.1002/anie.200605205
2,6-dimethyl-hepta-1,6-diene	dichloromethane	N Parameter: 1.69 s_N Parameter: 1.00	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
2,5-dimethylpyrrole	MeCN	N Parameter: 8.01 s_N Parameter: 0.96	Eur. J. Org. Chem. 2008, , 2369-2374 DOI: 10.1002/ejoc.200800092
2,5-dimethylindole	MeCN	N Parameter: 7.22 s_N Parameter: 1.10	J. Org. Chem. 2006, 71, 9088-9095 DOI: 10.1021/jo0614339
2,5-dimethyl-hexa-1,5-diene	dichloromethane	N Parameter: 1.14 s_N Parameter: 1.00	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
2,4-dimethylpyrrole	MeCN	N Parameter: 10.67 s_N Parameter: 0.91	Eur. J. Org. Chem. 2008, , 2369-2374 DOI: 10.1002/ejoc.200800092
2,4-dimethyl-penta-1,4-diene	dichloromethane	N Parameter: 0.54 s_N Parameter: 1.00	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
2,4,6-trimethylstyrene	dichloromethane	N Parameter: 0.68 s_N Parameter: 1.09	Macromolecules 2005, 38, 33-40 DOI: 10.1021/ma048389o
2,4,4-trimethyl-pent-1-ene	dichloromethane	N Parameter: 0.79 s_N Parameter: 1.07	J. Am. Chem. Soc. 2012, 134, 13902-13911 DOI: 10.1021/ja306522b
2,3-dimethyl-buta-1,3-diene	dichloromethane	N Parameter: 1.17 s_N Parameter: 1.00	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
2,3-dimethyl-but-1-ene	dichloromethane	N Parameter: 0.65 s_N Parameter: 1.00	J. Am. Chem. Soc. 2012, 134, 13902-13911 DOI: 10.1021/ja306522b
2,3-dihydrofuran	dichloromethane	N Parameter: 4.37 s_N Parameter: 0.90	Eur. J. Org. Chem. 2005, , 1760-1764 DOI: 10.1002/ejoc.200400706
2,3,3-trimethyl-but-1-ene	dichloromethane	N Parameter: 0.06 s_N Parameter: 1.07	J. Am. Chem. Soc. 2012, 134, 13902-13911 DOI: 10.1021/ja306522b
2,2-dimethyl-5-(4-nitrobenzyl)-4,6-dioxo-1,3-dioxan-5-ide (in DMSO)	DMSO	N Parameter: 12.02 s_N Parameter: 1.17	Chem. Eur. J. 2014, 20, 11069-11077 DOI: 10.1002/chem.201403161
1H-indole-5-carboxylic acid	MeCN	N Parameter: 3.97 s_N Parameter: 1.10	J. Org. Chem. 2006, 71, 9088-9095 DOI: 10.1021/jo0614339
1-pyrrolidino-3,4-dihydronaphthalene (in MeCN)	MeCN	N Parameter: 14.09 s_N Parameter: 0.66	Synthesis 2019, 51, 1157-1170 DOI: 10.1055/s-0037-1611634
1-phenyl-1-(trimethylsiloxy)ethene	dichloromethane	N Parameter: 6.22 s_N Parameter: 0.96	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
1-phenoxy-1-(trimethylsiloxy)ethene	dichloromethane	N Parameter: 8.23 s_N Parameter: 0.81	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
1-methylcyclopentene	dichloromethane	N Parameter: 1.18 s_N Parameter: 1.17	J. Am. Chem. Soc. 2012, 134, 13902-13911 DOI: 10.1021/ja306522b
1-methylcyclohexene	dichloromethane	N Parameter: 0.08 s_N Parameter: 1.15	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
1-methyl-4-vinyl-benzene	dichloromethane	N Parameter: 1.70 s_N Parameter: 1.06	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
1-methyl-4-(N-morpholino)tetrahydropyridine	dichloromethane	N Parameter: 12.03 s_N Parameter: 0.80	Chem. Eur. J. 2003, 9, 2209-2218 DOI: 10.1002/chem.200204666
1-methyl-2-methylene-3-phenyl-1,2-dihydropyridine (in DMSO)	DMSO	N Parameter: 19.41 s_N Parameter: 0.61	Eur. J. Org. Chem. 2024, , EarlyView DOI: 10.1002/ejoc.202400373
1-methoxy-2-methyl-1-(trimethylsiloxy)propene (in MeCN)	MeCN	N Parameter: 9.11 s_N Parameter: 0.88	J. Am. Chem. Soc. 2013, 135, 6579-6587 DOI: 10.1021/ja401106x
1-methoxy-2-methyl-1-(trimethylsiloxy)propene	dichloromethane	N Parameter: 9.00 s_N Parameter: 0.98	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
1-mesityl-3-methyl-5-methylene-2,4,6-triphenyl-2,5-dihydropyridin-1-ium-2-ide (in THF)	THF	N Parameter: 26.16 s_N Parameter: 0.52	Angew. Chem. Int. Ed. 2024, , e202318283 DOI: 10.1002/anie.202318283
1-hexene	dichloromethane	N Parameter: -2.77 s_N Parameter: 1.41	J. Am. Chem. Soc. 2012, 134, 13902-13911 DOI: 10.1021/ja306522b
1-ethoxy-3-(4-nitrophenyl)-1,3-dioxopropan-2-ide (in DMSO)	DMSO	N Parameter: 16.26 s_N Parameter: 0.83	J. Am. Chem. Soc. 2018, 140, 11474-11486 DOI: 10.1021/jacs.8b07147
1-ethoxy-2-methyl-1,3-dioxobutan-2-ide (in DMSO)	DMSO	N Parameter: 19.58 s_N Parameter: 0.73	Eur. J. Org. Chem. 2015, , 7594-7601 DOI: 10.1002/ejoc.201501107
1-ethinylcyclohexenyl-Co2(CO)6	dichloromethane	N Parameter: -0.44 s_N Parameter: 1.06	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
1-butoxy-1-(trimethylsiloxy)ethene	dichloromethane	N Parameter: 10.21 s_N Parameter: 0.82	Eur. J. Org. Chem. 2004, , 2791-2796 DOI: 10.1002/ejoc.200400134
1-butoxy-1-(t-butyl-dimethylsiloxy)ethene	dichloromethane	N Parameter: 10.32 s_N Parameter: 0.79	Eur. J. Org. Chem. 2004, , 2791-2796 DOI: 10.1002/ejoc.200400134
1-(tris(trimethylsilyl)siloxy)cyclohexene	dichloromethane	N Parameter: 5.07 s_N Parameter: 0.91	Org. Lett. 2010, 12, 5206-5209 DOI: 10.1021/ol102220e
1-(tris(pentafluorophenyl)siloxy)-cyclopentene	dichloromethane	N Parameter: 1.38 s_N Parameter: 0.93	Eur. J. Org. Chem. 2005, , 1760-1764 DOI: 10.1002/ejoc.200400706
1-(triphenylsiloxy)cyclopentene	dichloromethane	N Parameter: 5.76 s_N Parameter: 1.02	Eur. J. Org. Chem. 2005, , 1760-1764 DOI: 10.1002/ejoc.200400706
1-(trimethylsiloxy)cyclopentene (in MeCN)	MeCN	N Parameter: 6.43 s_N Parameter: 0.89	Chem. Asian J. 2012, 7, 1401-1407 DOI: 10.1002/asia.201101046
1-(trimethylsiloxy)cyclopentene	dichloromethane	N Parameter: 6.57 s_N Parameter: 0.93	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
1-(trimethylsiloxy)cyclooctene	dichloromethane	N Parameter: 6.77 s_N Parameter: 1.00	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
1-(trimethylsiloxy)cyclohexene	dichloromethane	N Parameter: 5.21 s_N Parameter: 1.00	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
1-(trimethylsiloxy)cycloheptene	dichloromethane	N Parameter: 6.62 s_N Parameter: 1.00	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
1-(trimethylsiloxy)buta-1,3-diene	dichloromethane	N Parameter: 4.60 s_N Parameter: 0.90	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
1-(trimethylsiloxy)-3,4-dihydronaphthalene (in MeCN)	MeCN	N Parameter: 5.06 s_N Parameter: 0.91	Synthesis 2019, 51, 1157-1170 DOI: 10.1055/s-0037-1611634
1-(phenylmethylamino)cyclopentene	dichloromethane	N Parameter: 12.90 s_N Parameter: 0.79	Chem. Eur. J. 2003, 9, 2209-2218 DOI: 10.1002/chem.200204666
1-(phenylmethylamino)cyclohexene	dichloromethane	N Parameter: 10.73 s_N Parameter: 0.81	Chem. Eur. J. 2003, 9, 2209-2218 DOI: 10.1002/chem.200204666
1-(phenylethynyl)pyrrolidin-2-one	dichloromethane	N Parameter: 3.12 s_N Parameter: 0.85	Angew. Chem. Int. Ed. 2014, 53, 4968-4971 DOI: 10.1002/anie.201402055
1-(perfluorophenyl)-1-(trimethylsiloxy)ethene	dichloromethane	N Parameter: 1.47 s_N Parameter: 0.89	Org. Lett. 2012, 14, 3990-3993 DOI: 10.1021/ol301766w
1-(p-tolyl)-1-(trimethylsilyl)ethene	dichloromethane	N Parameter: -0.65 s_N Parameter: 1.59	Chem. Eur. J. 2014, 20, 1103-1110 DOI: 10.1002/chem.201303215
1-(N-pyrrolidino)cyclopentene	dichloromethane	N Parameter: 15.91 s_N Parameter: 0.86	Chem. Eur. J. 2003, 9, 2209-2218 DOI: 10.1002/chem.200204666
1-(N-pyrrolidino)cyclohexene (in MeCN)	MeCN	N Parameter: 16.42 s_N Parameter: 0.70	Angew. Chem. Int. Ed. 2010, 49, 9526-9529 DOI: 10.1002/anie.201004344
1-(N-pyrrolidino)cyclohexene	dichloromethane	N Parameter: 14.91 s_N Parameter: 0.86	Chem. Eur. J. 2003, 9, 2209-2218 DOI: 10.1002/chem.200204666
1-(N-piperidino)cyclopentene	dichloromethane	N Parameter: 15.06 s_N Parameter: 0.82	Chem. Eur. J. 2003, 9, 2209-2218 DOI: 10.1002/chem.200204666
1-(N-piperidino)cyclohexene (in MeCN)	MeCN	N Parameter: 14.02 s_N Parameter: 0.76	J. Am. Chem. Soc. 2013, 135, 6579-6587 DOI: 10.1021/ja401106x
1-(N-piperidino)cyclohexene	dichloromethane	N Parameter: 13.36 s_N Parameter: 0.81	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
1-(N-morpholino)cyclopentene	dichloromethane	N Parameter: 13.41 s_N Parameter: 0.82	Chem. Eur. J. 2003, 9, 2209-2218 DOI: 10.1002/chem.200204666
1-(N-morpholino)cyclohexene	dichloromethane	N Parameter: 11.40 s_N Parameter: 0.83	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
1-(isoquinolin-2-ium-2-yl)-2-oxo-2-phenylethan-1-ide (in DMSO)	DMSO	N Parameter: 20.08 s_N Parameter: 0.57	J. Am. Chem. Soc. 2013, 135, 15216-15224 DOI: 10.1021/ja407885h
1-(ethoxycarbonyl)-2-oxocyclopentan-1-ide (in DMSO)	DMSO	N Parameter: 18.63 s_N Parameter: 0.82	Eur. J. Org. Chem. 2015, , 7594-7601 DOI: 10.1002/ejoc.201501107
1-(ethoxycarbonyl)-2-oxocyclooctan-1-ide (in DMSO)	DMSO	N Parameter: 20.02 s_N Parameter: 0.76	Eur. J. Org. Chem. 2015, , 7594-7601 DOI: 10.1002/ejoc.201501107
1-(ethoxycarbonyl)-2-oxocyclohexan-1-ide (in DMSO)	DMSO	N Parameter: 18.32 s_N Parameter: 0.84	Eur. J. Org. Chem. 2015, , 7594-7601 DOI: 10.1002/ejoc.201501107
1-(ethoxycarbonyl)-2-oxocycloheptan-1-ide	DMSO	N Parameter: 19.53 s_N Parameter: 0.83	Eur. J. Org. Chem. 2015, , 7594-7601 DOI: 10.1002/ejoc.201501107
1-(ethoxycarbonyl)-2-oxocyclododecan-1-ide (in DMSO)	DMSO	N Parameter: 20.60 s_N Parameter: 0.63	Eur. J. Org. Chem. 2015, , 7594-7601 DOI: 10.1002/ejoc.201501107
1-(benzylideneamino)-2-ethoxy-2-oxoethan-1-ide (in DMSO)	DMSO	N Parameter: 29.10 s_N Parameter: 0.50	Tetrahedron 2019, 75, 459-463 DOI: 10.1016/j.tet.2018.11.075
1-(4-(tert-butyl)phenyl)-2-methylene-4,6-diphenyl-1,2-dihydropyridine (in DMSO)	DMSO	N Parameter: 19.36 s_N Parameter: 0.68	Eur. J. Org. Chem. 2024, , EarlyView DOI: 10.1002/ejoc.202400373
1-(4-(dimethylamino)pyridin-1-ium-1-yl)-2-oxo-2-phenylethan-1-ide (in DMSO)	DMSO	N Parameter: 21.61 s_N Parameter: 0.58	J. Am. Chem. Soc. 2013, 135, 15216-15224 DOI: 10.1021/ja407885h
1-(3-chloropyridin-1-ium-1-yl)-2-oxo-2-phenylethan-1-ide (in DMSO)	DMSO	N Parameter: 17.98 s_N Parameter: 0.63	J. Am. Chem. Soc. 2013, 135, 15216-15224 DOI: 10.1021/ja407885h
1-(1-cyclohexenyl)-4-methylpiperazine	dichloromethane	N Parameter: 12.51 s_N Parameter: 0.80	Chem. Eur. J. 2003, 9, 2209-2218 DOI: 10.1002/chem.200204666
1-((diphenylmethylene)amino)-2-ethoxy-2-oxoethan-1-ide (in DMSO)	DMSO	N Parameter: 26.95 s_N Parameter: 0.52	Tetrahedron 2019, 75, 459-463 DOI: 10.1016/j.tet.2018.11.075
1-((4-chlorobenzylidene)amino)-2-ethoxy-2-oxoethan-1-ide (in DMSO)	DMSO	N Parameter: 29.02 s_N Parameter: 0.49	Tetrahedron 2019, 75, 459-463 DOI: 10.1016/j.tet.2018.11.075
1,6-dimethyl-2-methylene-1,2-dihydropyridine (in DMSO)	DMSO	N Parameter: 20.76 s_N Parameter: 0.60	Eur. J. Org. Chem. 2024, , EarlyView DOI: 10.1002/ejoc.202400373
1,3-dimethylbarbiturate anion (in DMSO)	DMSO	N Parameter: 17.46 s_N Parameter: 0.72	J. Org. Chem. 2017, 82, 8476-8488 DOI: 10.1021/acs.joc.7b01223
1,3-dimethyl-2-methyleneimidazolidine (in THF)	THF	N Parameter: 18.11 s_N Parameter: 0.68	J. Org. Chem. 2021, 86, 2974-2985 DOI: 10.1021/acs.joc.0c02838
1,3-dimethyl-2-methylenehexahydropyrimidine (in THF)	THF	N Parameter: 18.68 s_N Parameter: 0.63	J. Org. Chem. 2021, 86, 2974-2985 DOI: 10.1021/acs.joc.0c02838
1,3-dimethyl-2-methylene-2,3-dihydro-1H-benzo[d]imidazole	THF	N Parameter: 19.84 s_N Parameter: 0.58	J. Org. Chem. 2021, 86, 2974-2985 DOI: 10.1021/acs.joc.0c02838
1,3-dimethyl-2-methylene-1,2-dihydropyridine (in MeCN)	MeCN	N Parameter: 19.69 s_N Parameter: 0.61	Eur. J. Org. Chem. 2024, , EarlyView DOI: 10.1002/ejoc.202400373
1,3-dimethyl-2-methylene-1,2-dihydropyridine (in DMSO)	DMSO	N Parameter: 19.91 s_N Parameter: 0.62	Eur. J. Org. Chem. 2024, , EarlyView DOI: 10.1002/ejoc.202400373
1,3-dimethoxybenzene	dichloromethane	N Parameter: 2.48 s_N Parameter: 1.09	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
1,3-dimesityl-4,5-dihydro-1H-imidazol-3-ium-2-ide (in THF)	THF	N Parameter: 23.35 s_N Parameter: 0.40	Angew. Chem. Int. Ed. 2011, 50, 6915-6919 DOI: 10.1002/anie.201102435
1,3-dimesityl-2-methylene-2,3-dihydro-1H-imidazole (in THF)	THF	N Parameter: 17.80 s_N Parameter: 0.79	J. Org. Chem. 2021, 86, 2974-2985 DOI: 10.1021/acs.joc.0c02838
1,3-dimesityl-1H-imidazol-3-ium-2-ide (in THF)	THF	N Parameter: 21.72 s_N Parameter: 0.45	Angew. Chem. Int. Ed. 2011, 50, 6915-6919 DOI: 10.1002/anie.201102435
1,3-Diisopropyl-4-methylene-5-phenyl-4,5-dihydro-1H-1,2,3-triazol-3-ium-5-ide (in THF)	THF	N Parameter: 30.25 s_N Parameter: 0.54	Angew. Chem. Int. Ed. 2023, 62, e202309790 DOI: 10.1002/anie.202309790
1,3-diethyl-thiobarbiturate anion (in DMSO)	DMSO	N Parameter: 14.90 s_N Parameter: 0.80	J. Org. Chem. 2017, 82, 8476-8488 DOI: 10.1021/acs.joc.7b01223
1,3-diethoxy-2-fluoro-1,3-dioxopropan-2-ide (in DMSO)	DMSO	N Parameter: 20.63 s_N Parameter: 0.76	Angew. Chem. Int. Ed. 2016, 55, 12845-12848 DOI: 10.1002/anie.201605616
1,3-Bis(2,6-diisopropylphenyl)-5-methylene-4-(2,4,6-triisopropylphenyl)-4,5-dihydro-1H-1,2,3-triazol-3-ium-4-ide (in THF)	THF	N Parameter: 21.36 s_N Parameter: 0.42	Angew. Chem. Int. Ed. 2023, 62, e202309790 DOI: 10.1002/anie.202309790
1,3-Bis(2,6-diisopropylphenyl)-5-methylene-4-(2,4,6-triisopropylphenyl)-4,5-dihydro-1H-1,2,3-triazol-3-ium-4-ide (in THF)	THF	N Parameter: 20.78 s_N Parameter: 0.61	Angew. Chem. Int. Ed. 2023, 62, e202309790 DOI: 10.1002/anie.202309790
1,3-bis(2,6-diisopropylphenyl)-5-methyl-4-methylene-4,5-dihydro-1H-1,2,3-triazol-3-ium-5-ide (in THF)	THF	N Parameter: 24.86 s_N Parameter: 0.52	Angew. Chem. Int. Ed. 2023, 62, e202309790 DOI: 10.1002/anie.202309790
1,3-Bis(2,6-diisopropylphenyl)-5-(4-methoxyphenyl)-4-methylene-4,5-dihydro-1H-1,2,3-triazol-3-ium-5-ide (in THF)	THF	N Parameter: 23.55 s_N Parameter: 0.56	Angew. Chem. Int. Ed. 2023, 62, e202309790 DOI: 10.1002/anie.202309790
1,3-bis(2,6-diisopropylphenyl)-4-methylene-5-phenyl-4,5-dihydro-1H-1,2,3-triazol-3-ium-5-ide (in THF)	THF	N Parameter: 22.80 s_N Parameter: 0.60	Angew. Chem. Int. Ed. 2023, 62, e202309790 DOI: 10.1002/anie.202309790
1,3-Bis(2,6-diisopropylphenyl)-4-methylene-5-(4-(trifluoromethyl)phenyl)-4,5-dihydro-1H-1,2,3-triazol-3-ium-5-ide (in THF)	THF	N Parameter: 22.30 s_N Parameter: 0.49	Angew. Chem. Int. Ed. 2023, 62, e202309790 DOI: 10.1002/anie.202309790
1,3,5-trimethyl-2-methylene-1,2-dihydropyridine (in DMSO)	DMSO	N Parameter: 21.16 s_N Parameter: 0.59	Eur. J. Org. Chem. 2024, , EarlyView DOI: 10.1002/ejoc.202400373
1,3,4-triphenyl-1H-1,2,4-triazol-4-ium-5-ide (in THF)	THF	N Parameter: 14.07 s_N Parameter: 0.84	Angew. Chem. Int. Ed. 2011, 50, 6915-6919 DOI: 10.1002/anie.201102435
1,2-dimethylindole	dichloromethane	N Parameter: 6.54 s_N Parameter: 1.10	J. Org. Chem. 2006, 71, 9088-9095 DOI: 10.1021/jo0614339
1,2-bis(trimethylsiloxy)cyclohexene	dichloromethane	N Parameter: 4.46 s_N Parameter: 1.15	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
1,2,5-trimethylpyrrole	MeCN	N Parameter: 8.69 s_N Parameter: 1.07	Eur. J. Org. Chem. 2008, , 2369-2374 DOI: 10.1002/ejoc.200800092
1,2,3-trimethoxy-1,3-dioxopropan-2-ide (in DMSO)	DMSO	N Parameter: 20.08 s_N Parameter: 0.74	Angew. Chem. Int. Ed. 2016, 55, 12845-12848 DOI: 10.1002/anie.201605616
1,1-dimethyl-2-methylenehydrazine (in CH2Cl2)	dichloromethane	N Parameter: 6.98 s_N Parameter: 0.85	Angew. Chem. Int. Ed. 2013, 52, 11900-11904 DOI: 10.1002/anie.201305092
1,1-diethoxyethene	dichloromethane	N Parameter: 9.81 s_N Parameter: 0.81	Eur. J. Org. Chem. 2004, , 2791-2796 DOI: 10.1002/ejoc.200400134
1,1-bis(trimethylsiloxy)propene	dichloromethane	N Parameter: 10.38 s_N Parameter: 0.87	Eur. J. Org. Chem. 2004, , 2791-2796 DOI: 10.1002/ejoc.200400134
(Z)-phenylpropene	dichloromethane	N Parameter: -1.07 s_N Parameter: 1.10	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
(Z)-penta-1,3-diene	dichloromethane	N Parameter: 0.66 s_N Parameter: 1.00	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
(Z)-but-2-enyltrimethylsilane	dichloromethane	N Parameter: 1.69 s_N Parameter: 1.10	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
(Z)-but-2-ene	dichloromethane	N Parameter: -2.44 s_N Parameter: 1.09	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
(Z)-2-phenyl-1-(1,3,4-triphenyl-4H-1,2,4-triazol-1-ium-5-yl)prop-1-en-1-olate (in THF)	THF	N Parameter: 14.40 s_N Parameter: 0.66	Angew. Chem. Int. Ed. 2013, 52, 11163-11167 DOI: 10.1002/ange.201303524
(Z)-1-phenyl-1-(trimethylsiloxy)propene (in MeCN)	MeCN	N Parameter: 5.18 s_N Parameter: 0.94	Synthesis 2019, 51, 1157-1170 DOI: 10.1055/s-0037-1611634
(Z)-1-(triisopropylsiloxy)propen	dichloromethane	N Parameter: 3.87 s_N Parameter: 1.00	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
(Z)-1-(N-morpholino)propene	dichloromethane	N Parameter: 12.26 s_N Parameter: 0.80	Chem. Eur. J. 2003, 9, 2209-2218 DOI: 10.1002/chem.200204666
(Z)-1-(1,3-dimesityl-4,5-dihydro-1H-imidazol-3-ium-2-yl)-2-phenylprop-1-en-1-olate (in THF)	THF	N Parameter: 15.92 s_N Parameter: 0.72	Angew. Chem. Int. Ed. 2013, 52, 11163-11167 DOI: 10.1002/ange.201303524
(Z)-1-(1,3-dimesityl-1H-imidazol-3-ium-2-yl)-2-phenylprop-1-en-1-olate (in THF)	THF	N Parameter: 15.33 s_N Parameter: 0.79	Angew. Chem. Int. Ed. 2013, 52, 11163-11167 DOI: 10.1002/ange.201303524
(Z)-1-(1,3-dimesityl-1H-imidazol-3-ium-2-yl)-2-phenylprop-1-en-1-olate (in DMSO)	DMSO	N Parameter: 14.40 s_N Parameter: 0.64	Angew. Chem. Int. Ed. 2013, 52, 11163-11167 DOI: 10.1002/ange.201303524
(Z)-1,2-diphenyl-1-(trimethylsiloxy)ethene (in MeCN)	MeCN	N Parameter: 3.00 s_N Parameter: 0.83	Synthesis 2019, 51, 1157-1170 DOI: 10.1055/s-0037-1611634
(tris(trimethylsilyl)siloxy)ethene	dichloromethane	N Parameter: 4.01 s_N Parameter: 0.83	Org. Lett. 2010, 12, 5206-5209 DOI: 10.1021/ol102220e
(trimethylsilyl)diazomethane	dichloromethane	N Parameter: 8.97 s_N Parameter: 0.75	Chem. Eur. J. 2003, 9, 4068-4076 DOI: 10.1002/chem.200304913
(triisopropylsiloxy)ethene	dichloromethane	N Parameter: 3.44 s_N Parameter: 0.94	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
(S,E)-5-benzyl-2,2,3-trimethyl-1-styrylimidazolidin-4-one	MeCN	N Parameter: 7.20 s_N Parameter: 1.14	Angew. Chem. Int. Ed. 2012, 51, 5739-5742 DOI: 10.1002/anie.201201240
(S,E)-3-benzyl-1-methyl-4-styryl-1,4-diazaspiro[4.4]nonan-2-one	MeCN	N Parameter: 7.92 s_N Parameter: 1.07	Angew. Chem. Int. Ed. 2012, 51, 5739-5742 DOI: 10.1002/anie.201201240
(S,E)-2-(diphenyl(trimethylsiloxy)methyl)-1-styrylpyrrolidine	MeCN	N Parameter: 10.56 s_N Parameter: 1.01	Angew. Chem. Int. Ed. 2012, 51, 5739-5742 DOI: 10.1002/anie.201201240
(p-nitrophenyl)diazomethane	dichloromethane	N Parameter: 7.17 s_N Parameter: 0.83	J. Am. Chem. Soc. 2018, 140, 16758-16772 DOI: 10.1021/jacs.8b09995
(p-cyanophenyl)diazomethane	dichloromethane	N Parameter: 7.66 s_N Parameter: 0.80	J. Am. Chem. Soc. 2018, 140, 16758-16772 DOI: 10.1021/jacs.8b09995
(p-bromophenyl)diazomethane	dichloromethane	N Parameter: 8.87 s_N Parameter: 0.82	J. Am. Chem. Soc. 2018, 140, 16758-16772 DOI: 10.1021/jacs.8b09995
(EtO)2P(O)CH(-)CO2Et (in DMSO)	DMSO	N Parameter: 19.23 s_N Parameter: 0.65	J. Am. Chem. Soc. 2009, 131, 704-714 DOI: 10.1021/ja8056216
(EtO)2P(O)CH(-)CN (in DMSO)	DMSO	N Parameter: 18.57 s_N Parameter: 0.66	J. Am. Chem. Soc. 2009, 131, 704-714 DOI: 10.1021/ja8056216
(E,E)-hexa-2,4-diene	dichloromethane	N Parameter: 1.17 s_N Parameter: 1.10	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
(E)-propenylbenzene	dichloromethane	N Parameter: -0.49 s_N Parameter: 1.18	J. Am. Chem. Soc. 2012, 134, 13902-13911 DOI: 10.1021/ja306522b
(E)-penta-1,3-diene	dichloromethane	N Parameter: 1.49 s_N Parameter: 1.00	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
(E)-but-2-enyltrimethylsilane	dichloromethane	N Parameter: 1.94 s_N Parameter: 1.10	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
(E)-but-2-ene	dichloromethane	N Parameter: -2.45 s_N Parameter: 1.10	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
(E)-beta-(N-piperidino)styrene (in MeCN)	MeCN	N Parameter: 13.84 s_N Parameter: 0.73	Chem. Eur. J. 2018, 24, 5901-5910 DOI: 10.1002/chem.201705962
(E)-beta-(N-morpholino)styrene	dichloromethane	N Parameter: 10.76 s_N Parameter: 0.87	Chem. Eur. J. 2003, 9, 2209-2218 DOI: 10.1002/chem.200204666
(E)-4-styrylmorpholine	MeCN	N Parameter: 11.66 s_N Parameter: 0.83	Chem. Eur. J. 2018, 24, 5901-5910 DOI: 10.1002/chem.201705962
(E)-4-(ethylthio)-2,2,5,5-tetramethyl-1-styryl-2,5-dihydro-1H-imidazole (in MeCN)	MeCN	N Parameter: 8.12 s_N Parameter: 0.88	Chem. Eur. J. 2024, 30, e202302764 DOI: 10.1002/chem.202302764
(E)-4-(ethylthio)-2,2,5,5-tetramethyl-1-styryl-2,5-dihydro-1H-imidazole (in CH2Cl2)	dichloromethane	N Parameter: 8.13 s_N Parameter: 0.97	Chem. Eur. J. 2024, 30, e202302764 DOI: 10.1002/chem.202302764
(E)-4-(ethylthio)-2,2,5,5-tetramethyl-1-(3-phenylprop-1-en-1-yl)-2,5-dihydro-1H-imidazole (in MeCN)	MeCN	N Parameter: 9.64 s_N Parameter: 0.70	Chem. Eur. J. 2024, 30, e202302764 DOI: 10.1002/chem.202302764
(E)-4-(ethylthio)-2,2,5,5-tetramethyl-1-(3-phenylbut-1-en-1-yl)-2,5-dihydro-1H-imidazole (in MeCN)	MeCN	N Parameter: 7.92 s_N Parameter: 0.73	Chem. Eur. J. 2024, 30, e202302764 DOI: 10.1002/chem.202302764
(E)-4-(benzylthio)-2,2,5,5-tetramethyl-1-styryl-2,5-dihydro-1H-imidazole (in MeCN)	MeCN	N Parameter: 8.30 s_N Parameter: 0.84	Chem. Eur. J. 2024, 30, e202302764 DOI: 10.1002/chem.202302764
(E)-4-(benzylthio)-2,2,5,5-tetramethyl-1-styryl-2,5-dihydro-1H-imidazole (in CH2Cl2)	dichloromethane	N Parameter: 7.99 s_N Parameter: 0.98	Chem. Eur. J. 2024, 30, e202302764 DOI: 10.1002/chem.202302764
(E)-4-(2-phenyl-2-(pyrrolidin-1-yl)vinyl)benzonitrile (in MeCN)	MeCN	N Parameter: 10.63 s_N Parameter: 0.84	Chem. Eur. J. 2018, 24, 5901-5910 DOI: 10.1002/chem.201705962
(E)-4-(1,2-diphenylvinyl)morpholine (in MeCN)	MeCN	N Parameter: 8.78 s_N Parameter: 0.83	Chem. Eur. J. 2018, 24, 5901-5910 DOI: 10.1002/chem.201705962
(E)-2-methyl-penta-1,3-diene	dichloromethane	N Parameter: 3.09 s_N Parameter: 1.00	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
(E)-2-((1-(but-1-en-1-yl)-2,2,5,5-tetramethyl-2,5-dihydro-1H-imidazol-4-yl)thio)acetonitrile (in MeCN)	MeCN	N Parameter: 9.23 s_N Parameter: 0.74	Chem. Eur. J. 2024, 30, e202302764 DOI: 10.1002/chem.202302764
(E)-2,2,3,5,5-pentamethyl-1-styrylimidazolidine-4-thione (in MeCN)	MeCN	N Parameter: 6.49 s_N Parameter: 0.83	Chem. Eur. J. 2024, 30, e202302764 DOI: 10.1002/chem.202302764
(E)-2,2,3,5,5-pentamethyl-1-styrylimidazolidin-4-one (in MeCN)	MeCN	N Parameter: 7.10 s_N Parameter: 0.82	Chem. Eur. J. 2024, 30, e202302764 DOI: 10.1002/chem.202302764
(E)-13-(ethylthio)-6-styryl-6,12-diazadispiro[4.1.47.25]tridec-12-ene (in MeCN)	MeCN	N Parameter: 7.79 s_N Parameter: 0.87	Chem. Eur. J. 2024, 30, e202302764 DOI: 10.1002/chem.202302764
(E)-1-styrylpyrrolidine (in MeCN)	MeCN	N Parameter: 13.87 s_N Parameter: 0.76	Chem. Eur. J. 2018, 24, 5901-5910 DOI: 10.1002/chem.201705962
(E)-1-styrylpyrrolidine (in CH2Cl2)	dichloromethane	N Parameter: 12.26 s_N Parameter: 0.93	J. Am. Chem. Soc. 2014, 136, 14263-14269 DOI: 10.1021/ja508065e
(E)-1-styryl-2-tritylpyrrolidine (in CH2Cl2)	dichloromethane	N Parameter: 10.19 s_N Parameter: 1.06	J. Am. Chem. Soc. 2014, 136, 14263-14269 DOI: 10.1021/ja508065e
(E)-1-styryl-2-(triphenylsilyl)pyrrolidine (in CH2Cl2)	dichloromethane	N Parameter: 11.77 s_N Parameter: 0.98	J. Am. Chem. Soc. 2014, 136, 14263-14269 DOI: 10.1021/ja508065e
(E)-1-(N-morpholino)propene	dichloromethane	N Parameter: 12.06 s_N Parameter: 0.80	Chem. Eur. J. 2003, 9, 2209-2218 DOI: 10.1002/chem.200204666
(E)-1-(2-(4-nitrophenyl)-1-phenylvinyl)pyrrolidine (in MeCN)	MeCN	N Parameter: 10.42 s_N Parameter: 0.82	Chem. Eur. J. 2018, 24, 5901-5910 DOI: 10.1002/chem.201705962
(E)-1-(2-(4-methoxyphenyl)-1-phenylvinyl)pyrrolidine (in MeCN)	MeCN	N Parameter: 11.99 s_N Parameter: 0.84	Chem. Eur. J. 2018, 24, 5901-5910 DOI: 10.1002/chem.201705962
(E)-1-(1,2-diphenylvinyl)pyrrolidine (in MeCN)	MeCN	N Parameter: 11.66 s_N Parameter: 0.82	Chem. Eur. J. 2018, 24, 5901-5910 DOI: 10.1002/chem.201705962
(E)-1-(1,2-diphenylvinyl)piperidine (in MeCN)	MeCN	N Parameter: 9.94 s_N Parameter: 0.86	Chem. Eur. J. 2018, 24, 5901-5910 DOI: 10.1002/chem.201705962
(cyclohexen-1-yl)prolinate (in MeCN)	MeCN	N Parameter: 18.86 s_N Parameter: 0.70	Angew. Chem. Int. Ed. 2010, 49, 9526-9529 DOI: 10.1002/anie.201004344
(Cp*)2Zr(Me)2 - Dimethyl-bis(pentamethylcyclopentadienyl)zirconium	dichloromethane	N Parameter: 5.49 s_N Parameter: 1.06	Chem. Eur. J. 2016, 22, 11196-11200 DOI: 10.1002/chem.201602452
(C6H5)-(CO)-CH=SMe2 (in DMSO)	DMSO	N Parameter: 13.95 s_N Parameter: 0.69	J. Am. Chem. Soc. 2010, 132, 17894-17900 DOI: 10.1021/ja1084749
(bis(trimethylsiloxy)amino)styrene	dichloromethane	N Parameter: 4.80 s_N Parameter: 0.86	J. Org. Chem. 2001, 66, 3196-3200 DOI: 10.1021/jo0015927
(allyl)dicarbonyl(cyclopentadienyl)iron(II)	dichloromethane	N Parameter: 6.78 s_N Parameter: 0.95	Helv. Chim. Acta 2005, 88, 1754-1768 DOI: 10.1002/hlca.200590137
(5-methyl-furan-2-yl)(1,1,1-tris(methoxy)ethane)borate	MeCN	N Parameter: 12.55 s_N Parameter: 0.92	Chem. Sci. 2012, 3, 878-882 DOI: 10.1039/c2sc00883a
(5-methyl-furan-2-yl) trifluoroborate	MeCN	N Parameter: 7.66 s_N Parameter: 1.04	Chem. Sci. 2012, 3, 878-882 DOI: 10.1039/c2sc00883a
(5-methyl-furan-2-yl) pinacol boronate	MeCN	N Parameter: 2.90 s_N Parameter: 0.98	Chem. Sci. 2012, 3, 878-882 DOI: 10.1039/c2sc00883a
(5-methyl-furan-2-yl) MIDA boronate	MeCN	N Parameter: 1.84 s_N Parameter: 1.26	Chem. Sci. 2012, 3, 878-882 DOI: 10.1039/c2sc00883a
(5-methyl-furan-2-yl) MDA boronate	MeCN	N Parameter: 6.38 s_N Parameter: 0.86	Chem. Sci. 2012, 3, 878-882 DOI: 10.1039/c2sc00883a
(4-MeO-C6H4)-(CO)-CH=SMe2 (in DMSO)	DMSO	N Parameter: 14.48 s_N Parameter: 0.71	J. Am. Chem. Soc. 2010, 132, 17894-17900 DOI: 10.1021/ja1084749
(4-Me2N-C6H4)-(CO)-CH=SMe2 (in DMSO)	DMSO	N Parameter: 15.68 s_N Parameter: 0.65	J. Am. Chem. Soc. 2010, 132, 17894-17900 DOI: 10.1021/ja1084749
(4-Br-C6H4)-(CO)-CH=SMe2 (in DMSO)	DMSO	N Parameter: 13.78 s_N Parameter: 0.72	J. Am. Chem. Soc. 2010, 132, 17894-17900 DOI: 10.1021/ja1084749
(4-Br-C6H4)-(CO)-CH=SMe2	dichloromethane	N Parameter: 11.95 s_N Parameter: 0.76	Angew. Chem. Int. Ed. 2009, 48, 5034-5037 DOI: 10.1002/anie.200900933
(3,3,4,4,5,5,6,6,7,7,7-undecafluoro)-2-(trimethylsiloxy)hept-1-ene	dichloromethane	N Parameter: -3.52 s_N Parameter: 1.17	Org. Lett. 2012, 14, 3990-3993 DOI: 10.1021/ol301766w
(2S,5S)-5-benzyl-2-(tert-butyl)-3-methyl-1-((E)-styryl)imidazolidin-4-one	MeCN	N Parameter: 5.80 s_N Parameter: 0.87	Angew. Chem. Int. Ed. 2012, 51, 5739-5742 DOI: 10.1002/anie.201201240
(2-methylallyl)tris(trimethylsilyl)silane	dichloromethane	N Parameter: 4.63 s_N Parameter: 0.87	Org. Lett. 2010, 12, 5206-5209 DOI: 10.1021/ol102220e
(2-methylallyl)triphenylstannane	dichloromethane	N Parameter: 5.13 s_N Parameter: 0.90	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
(2-methylallyl)triphenylsilane	dichloromethane	N Parameter: 4.17 s_N Parameter: 0.79	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
(2-methylallyl)triphenylgermane	dichloromethane	N Parameter: 4.67 s_N Parameter: 0.81	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
(2-methylallyl)trimethylsilane	dichloromethane	N Parameter: 4.41 s_N Parameter: 0.96	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
(2-methylallyl)trichlorosilane	dichloromethane	N Parameter: -0.57 s_N Parameter: 0.95	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
(2-methylallyl)tributylstannane	dichloromethane	N Parameter: 7.48 s_N Parameter: 0.89	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
(2-methylallyl)dicarbonyl(cyclopentadienyl)iron(II)	dichloromethane	N Parameter: 8.45 s_N Parameter: 0.83	Helv. Chim. Acta 2005, 88, 1754-1768 DOI: 10.1002/hlca.200590137
(2-methylallyl)benzene	dichloromethane	N Parameter: 0.25 s_N Parameter: 1.00	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
(2,3-dimethylbut-2-enyl)triethylsilane	dichloromethane	N Parameter: 3.15 s_N Parameter: 1.15	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
(1S)-(-)-alpha-pinene	dichloromethane	N Parameter: 0.68 s_N Parameter: 1.10	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
(1H-inden-1-yl)zinc(II) chloride*LiCl (in DMSO)	DMSO	N Parameter: 18.10 s_N Parameter: 0.46	Angew. Chem. Int. Ed. 2015, 54, 12497-12500 DOI: 10.1002/anie.201501385
(1H-inden-1-yl)zinc(II) bromide*LiBr (in DMSO)	DMSO	N Parameter: 15.60 s_N Parameter: 0.51	Angew. Chem. Int. Ed. 2015, 54, 12497-12500 DOI: 10.1002/anie.201501385
(1H-inden-1-yl)trimethylstannane (in CH2Cl2)	dichloromethane	N Parameter: 6.68 s_N Parameter: 0.81	Angew. Chem. Int. Ed. 2015, 54, 12497-12500 DOI: 10.1002/anie.201501385
(1H-inden-1-yl)trimethylsilane (in CH2Cl2)	dichloromethane	N Parameter: -0.10 s_N Parameter: 1.05	Angew. Chem. Int. Ed. 2015, 54, 12497-12500 DOI: 10.1002/anie.201501385
potassium trifluoro(furan-2-yl)borate	MeCN	N Parameter: 5.99 s_N Parameter: 0.79	J. Am. Chem. Soc. 2013, 135, 6317-6324 DOI: 10.1021/ja4017655
lithium (5-methylthiophen-2-yl)(4-(trifluoromethyl)phenyl)pinacolborate	MeCN	N Parameter: 6.24 s_N Parameter: 1.00	Angew. Chem. Int. Ed. 2015, 54, 2780-2783 DOI: 10.1002/anie.201410562