Electrophiles

Found 367 Molecules.

Molecule	Solvent	Reactivity Parameters	Reference (sort by title or year)
Umemoto I (triflate)	0	E Parameter: -13.08	Eur. J. Org. Chem. 2024, 27, e202400085 DOI: 10.1002/ejoc.202400085
Umemoto I (tetrafluoroborate)	0	E Parameter: -13.39	Eur. J. Org. Chem. 2024, 27, e202400085 DOI: 10.1002/ejoc.202400085
Umemoto II (triflate)	0	E Parameter: -12.80	Eur. J. Org. Chem. 2024, 27, e202400085 DOI: 10.1002/ejoc.202400085
(E)-6-(4-nitrobenzylidene)benzo[d][1,3]dioxol-5(6H)-one	0	E Parameter: -13.15	Chem. Eur. J. 2024, , e202403785 DOI: 10.1002/chem.202403785
(E)-6-(4-(trifluoromethyl)benzylidene)benzo[d][1,3]dioxol-5(6H)-one	0	E Parameter: -13.54	Chem. Eur. J. 2024, , e202403785 DOI: 10.1002/chem.202403785
(E)-6-(3-fluorobenzylidene)benzo[d][1,3]dioxol-5(6H)-one	0	E Parameter: -14.00	Chem. Eur. J. 2024, , e202403785 DOI: 10.1002/chem.202403785
(E)-6-(4-chlorobenzylidene)benzo[d][1,3]dioxol-5(6H)-one	0	E Parameter: -13.99	Chem. Eur. J. 2024, , e202403785 DOI: 10.1002/chem.202403785
(E)-6-benzylidenebenzo[d][1,3]dioxol-5(6H)-one	0	E Parameter: -14.47	Chem. Eur. J. 2024, , e202403785 DOI: 10.1002/chem.202403785
(E)-6-(4-methylbenzylidene)benzo[d][1,3]dioxol-5(6H)-one	0	E Parameter: -14.85	Chem. Eur. J. 2024, , e202403785 DOI: 10.1002/chem.202403785
(E)-6-(4-methoxybenzylidene)benzo[d][1,3]dioxol-5(6H)-one	0	E Parameter: -15.20	Chem. Eur. J. 2024, , e202403785 DOI: 10.1002/chem.202403785
(E)-6-(4-(dimethylamino)benzylidene)benzo[d][1,3]dioxol-5(6H)-one	0	E Parameter: -16.07	Chem. Eur. J. 2024, , e202403785 DOI: 10.1002/chem.202403785
(E)-6-(furan-2-ylmethylene)benzo[d][1,3]dioxol-5(6H)-one	0	E Parameter: -15.73	Org. Biomol. Chem. 2024, , accepted DOI: 10.1039/D4OB01855A
(E)-6-((1-methyl-1H-pyrrol-2-yl)methylene)benzo[d][1,3]dioxol-5(6H)-one	0	E Parameter: -17.03	Org. Biomol. Chem. 2024, , accepted DOI: 10.1039/D4OB01855A
(E)-6-((1-methyl-1H-indol-2-yl)methylene)benzo[d][1,3]dioxol-5(6H)-one	0	E Parameter: -15.55	Org. Biomol. Chem. 2024, , accepted DOI: 10.1039/D4OB01855A
(E)-6-((E)-3-phenylallylidene)benzo[d][1,3]dioxol-5(6H)-one	0	E Parameter: -16.00	Org. Biomol. Chem. 2024, , accepted DOI: 10.1039/D4OB01855A
methyl diazoacetate	0	E Parameter: -18.50	Chem. Eur. J. 2022, 28, e202201376 DOI: 10.1002/chem.202201376
dimethyl diazomalonate	0	E Parameter: -18.20	Chem. Eur. J. 2022, 28, e202201376 DOI: 10.1002/chem.202201376
(p-nitrophenyl)diazomethane	0	E Parameter: -18.30	Chem. Eur. J. 2022, 28, e202201376 DOI: 10.1002/chem.202201376
diphenyldiazomethane	0	E Parameter: -21.40	Chem. Eur. J. 2022, 28, e202201376 DOI: 10.1002/chem.202201376
3-methylcyclopentenone	DMSO	E Parameter: -28.90	Chem. Sci. 2021, 12, 4850-4865 DOI: 10.1039/D0SC06628A
2-methylcyclopentenone	DMSO	E Parameter: -22.10	Chem. Sci. 2021, 12, 4850-4865 DOI: 10.1039/D0SC06628A
cyclopentenone	DMSO	E Parameter: -20.60	Chem. Sci. 2021, 12, 4850-4865 DOI: 10.1039/D0SC06628A
furan-2(5H)-one	DMSO	E Parameter: -20.70	Chem. Sci. 2021, 12, 4850-4865 DOI: 10.1039/D0SC06628A
2-methylcyclohexenone	DMSO	E Parameter: -27.50	Chem. Sci. 2021, 12, 4850-4865 DOI: 10.1039/D0SC06628A
cyclohexenone	DMSO	E Parameter: -22.10	Chem. Sci. 2021, 12, 4850-4865 DOI: 10.1039/D0SC06628A
dihydro-2H-pyran-2-one	DMSO	E Parameter: -21.80	Chem. Sci. 2021, 12, 4850-4865 DOI: 10.1039/D0SC06628A
3-methylenetetrahydropyran-2-one	DMSO	E Parameter: -19.50	Chem. Sci. 2021, 12, 4850-4865 DOI: 10.1039/D0SC06628A
3-methylenedihydrofuranone	DMSO	E Parameter: -19.40	Chem. Sci. 2021, 12, 4850-4865 DOI: 10.1039/D0SC06628A
ethyl 3-nitro-1H-indole-1-carboxylate	0	E Parameter: -14.10	Chem. Commun. 2021, 57, 10071-10074 DOI: 10.1039/d1cc04074j
3-nitro-1-tosyl-1H-indole	0	E Parameter: -14.87	Chem. Commun. 2021, 57, 10071-10074 DOI: 10.1039/d1cc04074j
4-bromo-3-nitro-1-tosyl-1H-indole	0	E Parameter: -14.60	Chem. Commun. 2021, 57, 10071-10074 DOI: 10.1039/d1cc04074j
3-methylcyclohexenone	DMSO	E Parameter: -29.60	Chem. Sci. 2021, 12, 4850-4865 DOI: 10.1039/D0SC06628A
3,6-dinitro-1-tosyl-1H-indole	0	E Parameter: -12.90	Chem. Commun. 2021, 57, 10071-10074 DOI: 10.1039/d1cc04074j
cycloheptenone	DMSO	E Parameter: -22.00	Chem. Sci. 2021, 12, 4850-4865 DOI: 10.1039/D0SC06628A
(E)-2,6-di-tert-butyl-4-(3-phenylallylidene)cyclohexa-2,5-dien-1-one	DMSO	E Parameter: -17.00	Org. Lett. 2020, 22, 2182-2186 DOI: 10.1021/acs.orglett.0c00338
E)-2,6-di-tert-butyl-4-(3-(4-chlorophenyl)allylidene)cyclohexa-2,5-dien-1-one	DMSO	E Parameter: -16.84	Org. Lett. 2020, 22, 2182-2186 DOI: 10.1021/acs.orglett.0c00338
(E)-2,6-di-tert-butyl-4-(3-(4-nitrophenyl)allylidene)cyclohexa-2,5-dien-1-one	DMSO	E Parameter: -16.25	Org. Lett. 2020, 22, 2182-2186 DOI: 10.1021/acs.orglett.0c00338
(E)-2,6-di-tert-butyl-4-(3-(4-methoxyphenyl)allylidene)cyclohexa-2,5-dien-1-one	DMSO	E Parameter: -17.42	Org. Lett. 2020, 22, 2182-2186 DOI: 10.1021/acs.orglett.0c00338
2,6-di-tert-butyl-4-(2,2,2-trifluoroethylidene)cyclohexa-2,5-dien-1-one	DMSO	E Parameter: -11.68	Eur. J. Org. Chem. 2020, , 3812-3817 DOI: 10.1002/ejoc.202000295
phenyl isocyanate	MeCN	E Parameter: -15.38	J. Am. Chem. Soc. 2020, 142, 8383-8402 DOI: 10.1021/jacs.0c01960
p-tosyl isocyanate	MeCN	E Parameter: -7.69	J. Am. Chem. Soc. 2020, 142, 8383-8402 DOI: 10.1021/jacs.0c01960
phenyl isothiocyanate	DMSO	E Parameter: -18.15	J. Am. Chem. Soc. 2020, 142, 8383-8402 DOI: 10.1021/jacs.0c01960
p-nitrophenyl isothiocyanate	DMSO	E Parameter: -15.89	J. Am. Chem. Soc. 2020, 142, 8383-8402 DOI: 10.1021/jacs.0c01960
diphenylcarbodiimide	DMSO	E Parameter: -20.14	J. Am. Chem. Soc. 2020, 142, 8383-8402 DOI: 10.1021/jacs.0c01960
carbon disulfide	DMSO	E Parameter: -17.70	J. Am. Chem. Soc. 2020, 142, 8383-8402 DOI: 10.1021/jacs.0c01960
4-phenylbut-3-yn-2-one	0	E Parameter: -16.90	Angew. Chem. Int. Ed. 2019, 58, 17704-17708 DOI: 10.1002/anie.201909803
hex-3-yn-2-one	0	E Parameter: -17.90	Angew. Chem. Int. Ed. 2019, 58, 17704-17708 DOI: 10.1002/anie.201909803
butynone	0	E Parameter: -16.60	Angew. Chem. Int. Ed. 2019, 58, 17704-17708 DOI: 10.1002/anie.201909803
benzaldehyde (in DMSO)	DMSO	E Parameter: -12.90	J. Am. Chem. Soc. 2018, 140, 5500-5515 DOI: 10.1021/jacs.8b01657
2-cinnamoyl-3-methyl-1-(perfluorophenyl)-1H-imidazol-3-ium	DMSO	E Parameter: -10.09	Top. Catal. 2018, 61, 585-590 DOI: 10.1007/s11244-018-0914-5
1-(tert-butyl)-2-cinnamoyl-3-methyl-1H-imidazol-3-ium	DMSO	E Parameter: -11.80	Top. Catal. 2018, 61, 585-590 DOI: 10.1007/s11244-018-0914-5
2-cinnamoyl-1-mesityl-3-methyl-1H-imidazol-3-ium	DMSO	E Parameter: -11.48	Top. Catal. 2018, 61, 585-590 DOI: 10.1007/s11244-018-0914-5
2-cinnamoyl-1-(4-methoxyphenyl)-3-methyl-1H-imidazol-3-ium	DMSO	E Parameter: -11.79	Top. Catal. 2018, 61, 585-590 DOI: 10.1007/s11244-018-0914-5
2-cinnamoyl-1-(2,6-dimethoxyphenyl)-3-methyl-1H-imidazol-3-ium	DMSO	E Parameter: -12.02	Top. Catal. 2018, 61, 585-590 DOI: 10.1007/s11244-018-0914-5
cyclobutanone (in DMSO)	DMSO	E Parameter: -17.50	J. Am. Chem. Soc. 2018, 140, 5500-5515 DOI: 10.1021/jacs.8b01657
cyclopentanone (in DMSO)	DMSO	E Parameter: -21.00	J. Am. Chem. Soc. 2018, 140, 5500-5515 DOI: 10.1021/jacs.8b01657
cyclohexanone (in DMSO)	DMSO	E Parameter: -19.90	J. Am. Chem. Soc. 2018, 140, 5500-5515 DOI: 10.1021/jacs.8b01657
cycloheptanone (in DMSO)	DMSO	E Parameter: -22.10	J. Am. Chem. Soc. 2018, 140, 5500-5515 DOI: 10.1021/jacs.8b01657
1-methylpiperidin-4-one (in DMSO)	DMSO	E Parameter: -18.40	J. Am. Chem. Soc. 2018, 140, 5500-5515 DOI: 10.1021/jacs.8b01657
oxan-4-one (in DMSO)	DMSO	E Parameter: -17.90	J. Am. Chem. Soc. 2018, 140, 5500-5515 DOI: 10.1021/jacs.8b01657
thian-4-one (in DMSO)	DMSO	E Parameter: -16.90	J. Am. Chem. Soc. 2018, 140, 5500-5515 DOI: 10.1021/jacs.8b01657
1,4-dioxaspiro[4.5]decan-8-one (in DMSO)	DMSO	E Parameter: -18.20	J. Am. Chem. Soc. 2018, 140, 5500-5515 DOI: 10.1021/jacs.8b01657
pentan-2-one (in DMSO)	DMSO	E Parameter: -22.30	J. Am. Chem. Soc. 2018, 140, 5500-5515 DOI: 10.1021/jacs.8b01657
1-methylsulfanylpropan-2-one (in DMSO)	DMSO	E Parameter: -15.60	J. Am. Chem. Soc. 2018, 140, 5500-5515 DOI: 10.1021/jacs.8b01657
N-(phenylsulfonyl)-N-((trifluoromethyl)thio)benzenesulfonamide	0	E Parameter: -6.06	Angew. Chem. Int. Ed. 2018, 57, 12690-12695 DOI: 10.1002/anie.201805859
N-fluoro-2,4,6-trimethylpyridinium tetrafluoroborate	0	E Parameter: -10.46	J. Am. Chem. Soc. 2018, 140, 11474-11486 DOI: 10.1021/jacs.8b07147
N-fluoro-2,6-dichloropyridinium tetrafluoroborate	0	E Parameter: -5.29	J. Am. Chem. Soc. 2018, 140, 11474-11486 DOI: 10.1021/jacs.8b07147
Selectfluor	0	E Parameter: -5.20	J. Am. Chem. Soc. 2018, 140, 11474-11486 DOI: 10.1021/jacs.8b07147
NFSI	MeCN	E Parameter: -8.44	J. Am. Chem. Soc. 2018, 140, 11474-11486 DOI: 10.1021/jacs.8b07147
N-fluoropyridinium tetrafluoroborate	0	E Parameter: -9.89	J. Am. Chem. Soc. 2018, 140, 11474-11486 DOI: 10.1021/jacs.8b07147
N-(trifluoromethyl)thio)phthalimide	0	E Parameter: -11.92	Angew. Chem. Int. Ed. 2018, 57, 12690-12695 DOI: 10.1002/anie.201805859
N-(trifluoromethyl)thio)saccharin	0	E Parameter: -6.48	Angew. Chem. Int. Ed. 2018, 57, 12690-12695 DOI: 10.1002/anie.201805859
N-(trifluoromethyl)thio)succinimide	0	E Parameter: -12.56	Angew. Chem. Int. Ed. 2018, 57, 12690-12695 DOI: 10.1002/anie.201805859
N-(difluoromethyl)thio)phthalimide	0	E Parameter: -11.86	Angew. Chem. Int. Ed. 2018, 57, 12690-12695 DOI: 10.1002/anie.201805859
N-methyl-N-((trifluoromethyl)thio)-p-toluenesulfonamide	0	E Parameter: -13.44	Angew. Chem. Int. Ed. 2018, 57, 12690-12695 DOI: 10.1002/anie.201805859
N-methyl-N-((trifluoromethyl)thio)-aniline	0	E Parameter: -23.32	Angew. Chem. Int. Ed. 2018, 57, 12690-12695 DOI: 10.1002/anie.201805859
((2-phenylpropan-2-yl)oxy)(trifluoromethyl)sulfane	0	E Parameter: -13.77	Angew. Chem. Int. Ed. 2018, 57, 12690-12695 DOI: 10.1002/anie.201805859
((2-(2-iodophenyl)propan-2-yl)oxy)(trifluoromethyl)sulfane	0	E Parameter: -14.52	Angew. Chem. Int. Ed. 2018, 57, 12690-12695 DOI: 10.1002/anie.201805859
(E)-1,3-diphenylprop-2-en-1-one (in DMSO)	DMSO	E Parameter: -19.39	J. Am. Chem. Soc. 2017, 139, 13318-13329 DOI: 10.1021/jacs.7b05106
9-phenyl-9H-fluoren-9-ylium	dichloromethane	E Parameter: 2.41	Chem. Eur. J. 2017, 23, 623-630 DOI: 10.1002/chem.201603963
9-(4-methoxyphenyl)-9H-fluoren-9-ylium	dichloromethane	E Parameter: 0.85	Chem. Eur. J. 2017, 23, 623-630 DOI: 10.1002/chem.201603963
9-(4-(dimethylamino)phenyl)-9H-fluoren-9-ylium	dichloromethane	E Parameter: -4.51	Chem. Eur. J. 2017, 23, 623-630 DOI: 10.1002/chem.201603963
(E)-4-phenylbut-3-en-2-one (in DMSO)	DMSO	E Parameter: -23.01	J. Am. Chem. Soc. 2017, 139, 13318-13329 DOI: 10.1021/jacs.7b05106
cinnamonitrile (in DMSO)	DMSO	E Parameter: -24.60	J. Am. Chem. Soc. 2017, 139, 13318-13329 DOI: 10.1021/jacs.7b05106
methyl prop-2-enoate (in DMSO)	DMSO	E Parameter: -18.84	J. Am. Chem. Soc. 2017, 139, 13318-13329 DOI: 10.1021/jacs.7b05106
ethyl prop-2-enoate (in DMSO)	DMSO	E Parameter: -19.07	J. Am. Chem. Soc. 2017, 139, 13318-13329 DOI: 10.1021/jacs.7b05106
tert-butyl prop-2-enoate (in DMSO)	DMSO	E Parameter: -20.22	J. Am. Chem. Soc. 2017, 139, 13318-13329 DOI: 10.1021/jacs.7b05106
N,N-dimethylprop-2-enamide (in DMSO)	DMSO	E Parameter: -23.54	J. Am. Chem. Soc. 2017, 139, 13318-13329 DOI: 10.1021/jacs.7b05106
ethenylsulfonylbenzene (in DMSO)	DMSO	E Parameter: -18.36	J. Am. Chem. Soc. 2017, 139, 13318-13329 DOI: 10.1021/jacs.7b05106
acrylonitrile (in DMSO)	DMSO	E Parameter: -19.05	J. Am. Chem. Soc. 2017, 139, 13318-13329 DOI: 10.1021/jacs.7b05106
but-3-en-2-one (in DMSO)	DMSO	E Parameter: -16.76	J. Am. Chem. Soc. 2017, 139, 13318-13329 DOI: 10.1021/jacs.7b05106
1-phenylprop-2-en-1-one (in DMSO)	DMSO	E Parameter: -15.25	J. Am. Chem. Soc. 2017, 139, 13318-13329 DOI: 10.1021/jacs.7b05106
ethyl 2-methylprop-2-enoate (in DMSO)	DMSO	E Parameter: -22.77	J. Am. Chem. Soc. 2017, 139, 13318-13329 DOI: 10.1021/jacs.7b05106
ethyl (E)-but-2-enoate (in DMSO)	DMSO	E Parameter: -23.59	J. Am. Chem. Soc. 2017, 139, 13318-13329 DOI: 10.1021/jacs.7b05106
ethyl cinnamate (in DMSO)	DMSO	E Parameter: -24.52	J. Am. Chem. Soc. 2017, 139, 13318-13329 DOI: 10.1021/jacs.7b05106
(E)-1-methyl-4-(styrylsulfonyl)benzene (in DMSO)	DMSO	E Parameter: -24.69	J. Am. Chem. Soc. 2017, 139, 13318-13329 DOI: 10.1021/jacs.7b05106
ethenesulfonyl fluoride (ESF)	DMSO	E Parameter: -12.09	Angew. Chem. Int. Ed. 2016, 55, 12664-12667 DOI: 10.1002/anie.201601875
2-phenylethene-1-sulfonyl fluoride	DMSO	E Parameter: -16.63	Angew. Chem. Int. Ed. 2016, 55, 12664-12667 DOI: 10.1002/anie.201601875
(E)-2-(tert-butyl)-3-(4-methylbenzylidene)-3H-indol-1-ium	dichloromethane	E Parameter: -5.06	Eur. J. Org. Chem. 2016, , 4050-4058 DOI: 10.1002/ejoc.201600572
3-benzylidene-1-methyl-3H-indol-1-ium ion	0	E Parameter: -1.80	J. Org. Chem. 2015, 80, 8643-8656 DOI: 10.1021/acs.joc.5b01298
1-methyl-3-(4-methylbenzylidene)-3H-indol-1-ium ion	0	E Parameter: -2.19	J. Org. Chem. 2015, 80, 8643-8656 DOI: 10.1021/acs.joc.5b01298
3-(4-methoxybenzylidene)-1-methyl-3H-indol-1-ium iom	0	E Parameter: -3.02	J. Org. Chem. 2015, 80, 8643-8656 DOI: 10.1021/acs.joc.5b01298
3-(4-(dimethylamino)benzylidene)-1-methyl-3H-indol-1-ium ion	0	E Parameter: -6.26	J. Org. Chem. 2015, 80, 8643-8656 DOI: 10.1021/acs.joc.5b01298
1-methyl-3-((julolidin-9-yl)methylene)-3H-indol-1-ium ion	0	E Parameter: -7.79	J. Org. Chem. 2015, 80, 8643-8656 DOI: 10.1021/acs.joc.5b01298
(E)-2-methyl-3-(4-methylbenzylidene)-3H-indol-1-ium ion	0	E Parameter: -5.15	J. Org. Chem. 2015, 80, 8643-8656 DOI: 10.1021/acs.joc.5b01298
(E)-1,2-dimethyl-3-(4-methylbenzylidene)-3H-indol-1-ium ion	0	E Parameter: -5.05	J. Org. Chem. 2015, 80, 8643-8656 DOI: 10.1021/acs.joc.5b01298
(E)-3-benzylidene-1,2-dimethyl-3H-indol-1-ium ion	0	E Parameter: -4.96	J. Org. Chem. 2015, 80, 8643-8656 DOI: 10.1021/acs.joc.5b01298
bis(1-methylindol-3-yl)methylium ion	0	E Parameter: -5.99	J. Org. Chem. 2015, 80, 8643-8656 DOI: 10.1021/acs.joc.5b01298
bis(5-methoxy-1-methylindol-3-yl)methylium ion	0	E Parameter: -6.90	J. Org. Chem. 2015, 80, 8643-8656 DOI: 10.1021/acs.joc.5b01298
bis(1,2-dimethylindol-3-yl)methylium ion	0	E Parameter: -10.23	J. Org. Chem. 2015, 80, 8643-8656 DOI: 10.1021/acs.joc.5b01298
maleic anhydride	DMSO	E Parameter: -11.31	Eur. J. Org. Chem. 2014, , 2956-2963 DOI: 10.1002/ejoc.201301779
N-methyl maleimide	DMSO	E Parameter: -14.07	Eur. J. Org. Chem. 2014, , 2956-2963 DOI: 10.1002/ejoc.201301779
fumaronitrile	DMSO	E Parameter: -15.71	Eur. J. Org. Chem. 2014, , 2956-2963 DOI: 10.1002/ejoc.201301779
diethyl fumarate	DMSO	E Parameter: -17.79	Eur. J. Org. Chem. 2014, , 2956-2963 DOI: 10.1002/ejoc.201301779
diethyl maleate	DMSO	E Parameter: -19.49	Eur. J. Org. Chem. 2014, , 2956-2963 DOI: 10.1002/ejoc.201301779
(S,E)-5-benzyl-2,2,3-trimethyl-1-((E)-3-(4-nitrophenyl)allylidene)-4-oxoimidazolidin-1-ium	dichloromethane	E Parameter: -5.90	Asian J. Org. Chem. 2014, 3, 550-555 DOI: 10.1002/ajoc.201402009
(S,E)-5-benzyl-1-((E)-3-(4-cyanophenyl)allylidene)-2,2,3-trimethyl-4-oxoimidazolidin-1-ium	dichloromethane	E Parameter: -6.00	Asian J. Org. Chem. 2014, 3, 550-555 DOI: 10.1002/ajoc.201402009
(S,E)-5-benzyl-1-((E)-3-(4-(dimethylamino)phenyl)allylidene)-2,2,3-trimethyl-4-oxoimidazolidin-1-ium	dichloromethane	E Parameter: -10.60	Asian J. Org. Chem. 2014, 3, 550-555 DOI: 10.1002/ajoc.201402009
(S,E)-5-benzyl-2,2,3-trimethyl-4-oxo-1-((E)-3-(p-tolyl)allylidene)imidazolidin-1-ium	dichloromethane	E Parameter: -7.20	Asian J. Org. Chem. 2014, 3, 550-555 DOI: 10.1002/ajoc.201402009
(S,E)-5-benzyl-1-((E)-3-(4-methoxyphenyl)allylidene)-2,2,3-trimethyl-4-oxoimidazolidin-1-ium	dichloromethane	E Parameter: -8.00	Asian J. Org. Chem. 2014, 3, 550-555 DOI: 10.1002/ajoc.201402009
(S,E)-5-benzyl-2,2,3-trimethyl-1-((E)-3-(3-nitrophenyl)allylidene)-4-oxoimidazolidin-1-ium	dichloromethane	E Parameter: -6.10	Asian J. Org. Chem. 2014, 3, 550-555 DOI: 10.1002/ajoc.201402009
(S,E)-5-((1H-indol-3-yl)methyl)-2,2,3-trimethyl-4-oxo-1-((E)-3-phenylallylidene)imidazolidin-1-ium	dichloromethane	E Parameter: -7.30	Asian J. Org. Chem. 2014, 3, 550-555 DOI: 10.1002/ajoc.201402009
(2S,5S)-5-benzyl-3-methyl-4-oxo-1-(3-phenylallylidene)-2-((E)-styryl)imidazolidin-1-ium	dichloromethane	E Parameter: -5.90	Asian J. Org. Chem. 2014, 3, 550-555 DOI: 10.1002/ajoc.201402009
p-quinone (C-H)	0	E Parameter: -16.19	J. Am. Chem. Soc. 2014, 136, 11499-11512 DOI: 10.1021/ja505613b
2,5-dichloroquinone (C-H)	0	E Parameter: -12.28	J. Am. Chem. Soc. 2014, 136, 11499-11512 DOI: 10.1021/ja505613b
2,5-dichloroquinone (C-Cl)	0	E Parameter: -16.11	J. Am. Chem. Soc. 2014, 136, 11499-11512 DOI: 10.1021/ja505613b
p-chloranil (C=O)	0	E Parameter: -12.13	J. Am. Chem. Soc. 2014, 136, 11499-11512 DOI: 10.1021/ja505613b
p-chloranil (C-Cl)	0	E Parameter: -13.84	J. Am. Chem. Soc. 2014, 136, 11499-11512 DOI: 10.1021/ja505613b
p-fluoranil (C=O)	0	E Parameter: -9.37	J. Am. Chem. Soc. 2014, 136, 11499-11512 DOI: 10.1021/ja505613b
p-fluoranil (C-F)	0	E Parameter: -11.12	J. Am. Chem. Soc. 2014, 136, 11499-11512 DOI: 10.1021/ja505613b
o-chloranil (C=O)	0	E Parameter: -8.77	J. Am. Chem. Soc. 2014, 136, 11499-11512 DOI: 10.1021/ja505613b
o-chloranil (C-Cl)	0	E Parameter: -12.02	J. Am. Chem. Soc. 2014, 136, 11499-11512 DOI: 10.1021/ja505613b
PhCH=N+Me2 (in MeCN)	MeCN	E Parameter: -9.27	J. Am. Chem. Soc. 2013, 135, 6579-6587 DOI: 10.1021/ja401106x
pTolCH=N+CH2 (in MeCN)	MeCN	E Parameter: -9.64	J. Am. Chem. Soc. 2013, 135, 6579-6587 DOI: 10.1021/ja401106x
p-AniCH=N+Me2 (in MeCN)	MeCN	E Parameter: -10.69	J. Am. Chem. Soc. 2013, 135, 6579-6587 DOI: 10.1021/ja401106x
PhCH=N+(CH2)4 (in MeCN)	MeCN	E Parameter: -9.35	J. Am. Chem. Soc. 2013, 135, 6579-6587 DOI: 10.1021/ja401106x
PhCH=N+(CH2)5 (in MeCN)	MeCN	E Parameter: -9.60	J. Am. Chem. Soc. 2013, 135, 6579-6587 DOI: 10.1021/ja401106x
p-CF3-C6H4-CH=N+Me2 (in MeCN)	MeCN	E Parameter: -8.34	J. Am. Chem. Soc. 2013, 135, 6579-6587 DOI: 10.1021/ja401106x
(S,E)-2,2,3-trimethyl-4-oxo-5-((perfluorophenyl)methyl)-1-((E)-3-phenylallylidene)imidazolidin-1-ium	dichloromethane	E Parameter: -6.00	Angew. Chem. Int. Ed. 2013, 52, 7967-7971 DOI: 10.1002/anie.201301864
(S,E)-2,2,3-trimethyl-4-oxo-1-((E)-3-phenylallylidene)-5-(3,4,5-trimethoxybenzyl)imidazolidin-1-ium	dichloromethane	E Parameter: -7.00	Angew. Chem. Int. Ed. 2013, 52, 7967-7971 DOI: 10.1002/anie.201301864
2,3-dichloro-5,6-dicyano-p-benzoquinone (DDQ)	MeCN	E Parameter: -3.66	J. Am. Chem. Soc. 2013, 135, 12377-12387 DOI: 10.1021/ja405890d
benzhydrylium ion Ph2CH+	0	E Parameter: 5.47	J. Am. Chem. Soc. 2012, 134, 13902-13911 DOI: 10.1021/ja306522b
(pcp)2CH+	0	E Parameter: 5.48	J. Am. Chem. Soc. 2012, 134, 13902-13911 DOI: 10.1021/ja306522b
pfp(Ph)CH+	0	E Parameter: 5.20	J. Am. Chem. Soc. 2012, 134, 13902-13911 DOI: 10.1021/ja306522b
tol(Ph)CH+	0	E Parameter: 4.43	J. Am. Chem. Soc. 2012, 134, 13902-13911 DOI: 10.1021/ja306522b
(pfp)2CH+	0	E Parameter: 5.01	J. Am. Chem. Soc. 2012, 134, 13902-13911 DOI: 10.1021/ja306522b
(ethene-1,1-diyldisulfonyl)dibenzene	DMSO	E Parameter: -7.50	Chem. Asian J. 2012, 7, 1401-1407 DOI: 10.1002/asia.201101046
(2-phenylethene-1,1-diyldisulfonyl)dibenzene	DMSO	E Parameter: -12.93	Chem. Asian J. 2012, 7, 1401-1407 DOI: 10.1002/asia.201101046
(2-(4-methoxyphenyl)ethene-1,1-diyldisulfonyl)dibenzene	DMSO	E Parameter: -13.88	Chem. Asian J. 2012, 7, 1401-1407 DOI: 10.1002/asia.201101046
4-(2,2-bis(phenylsulfonyl)vinyl)-N,N-dimethylaniline	DMSO	E Parameter: -16.53	Chem. Asian J. 2012, 7, 1401-1407 DOI: 10.1002/asia.201101046
2-benzylidenebenzo[d][1,3]dithiole 1,1,3,3-tetraoxide	DMSO	E Parameter: -11.78	Chem. Asian J. 2012, 7, 1401-1407 DOI: 10.1002/asia.201101046
2-(4-methoxybenzylidene)benzo[d][1,3]dithiole 1,1,3,3-tetraoxide	DMSO	E Parameter: -13.02	Chem. Asian J. 2012, 7, 1401-1407 DOI: 10.1002/asia.201101046
2-(4-methoxybenzylidene)-1,3-dithiane 1,1,3,3-tetraoxide	DMSO	E Parameter: -14.55	Chem. Asian J. 2012, 7, 1401-1407 DOI: 10.1002/asia.201101046
[(1,3-Diarylallyl)Pd(PPh3)2]+ (Aryl = Ph)		E Parameter: -14.14	Organometallics 2012, 31, 2416-2424 DOI: 10.1021/om3000357
[(1,3-Diarylallyl)Pd(PPh3)2]+ (Aryl = 3,5-difluorophenyl)		E Parameter: -14.21	Organometallics 2012, 31, 2416-2424 DOI: 10.1021/om3000357
[(1,3-Diarylallyl)Pd(PPh3)2]+ (Aryl = 4-(dimethylamino)phenyl)		E Parameter: -14.46	Organometallics 2012, 31, 2416-2424 DOI: 10.1021/om3000357
2-cinnamoyl-1,3-dimethyl-1H-imidazol-3-ium	DMSO	E Parameter: -11.52	Angew. Chem. Int. Ed. 2012, 51, 5234-5238 DOI: 10.1002/anie.201109042
(fur)(ani)CH+	0	E Parameter: -0.81	J. Am. Chem. Soc. 2012, 134, 13902-13911 DOI: 10.1021/ja306522b
(mfp)PhCH+	0	E Parameter: 6.23	J. Am. Chem. Soc. 2012, 134, 13902-13911 DOI: 10.1021/ja306522b
(tfm)PhCH+	0	E Parameter: 6.70	J. Am. Chem. Soc. 2012, 134, 13902-13911 DOI: 10.1021/ja306522b
(dfp)PhCH+	0	E Parameter: 6.74	J. Am. Chem. Soc. 2012, 134, 13902-13911 DOI: 10.1021/ja306522b
(mfp)2CH+	0	E Parameter: 6.87	J. Am. Chem. Soc. 2012, 134, 13902-13911 DOI: 10.1021/ja306522b
(dfp)(mfp)CH+	0	E Parameter: 7.52	J. Am. Chem. Soc. 2012, 134, 13902-13911 DOI: 10.1021/ja306522b
(tfm)2CH+	0	E Parameter: 7.96	J. Am. Chem. Soc. 2012, 134, 13902-13911 DOI: 10.1021/ja306522b
(dfp)2CH+	0	E Parameter: 8.02	J. Am. Chem. Soc. 2012, 134, 13902-13911 DOI: 10.1021/ja306522b
(Ftol)2CH+	0	E Parameter: 5.24	J. Am. Chem. Soc. 2012, 134, 13902-13911 DOI: 10.1021/ja306522b
MacMillan-iminium ion (1st generation)	MeCN	E Parameter: -7.37	Angew. Chem. Int. Ed. 2011, 50, 9953-9956 DOI: 10.1002/anie.201103683
(4-MeO)-tritylium ion		E Parameter: -1.59	Eur. J. Org. Chem. 2011, , 6470-6475 DOI: 10.1002/ejoc.201100910
(E)-3-(4-nitro-phenyl)-1-phenyl-prop-2-en-1-one (in DMSO)	DMSO	E Parameter: -17.33	J. Am. Chem. Soc. 2011, 133, 8240-8251 DOI: 10.1021/ja200820m
(E)-3-(4-cyano-phenyl)-1-phenyl-prop-2-en-1-one (in DMSO)	DMSO	E Parameter: -17.64	J. Am. Chem. Soc. 2011, 133, 8240-8251 DOI: 10.1021/ja200820m
(E)-4-(4-nitrophenyl)but-3-en-2-one (in DSMO)	DMSO	E Parameter: -19.36	J. Am. Chem. Soc. 2011, 133, 8240-8251 DOI: 10.1021/ja200820m
(E)-4-methyl-1-(4-nitrophenyl)pent-1-en-3-one (in DMSO)	DMSO	E Parameter: -19.17	J. Am. Chem. Soc. 2011, 133, 8240-8251 DOI: 10.1021/ja200820m
(E)-4,4-dimethyl-1-(4-nitrophenyl)pent-1-en-3-one	DMSO	E Parameter: -19.15	J. Am. Chem. Soc. 2011, 133, 8240-8251 DOI: 10.1021/ja200820m
3-chloro-benzaldehyde (in DMSO)	DMSO		J. Am. Chem. Soc. 2011, 133, 8240-8251 DOI: 10.1021/ja200820m
3-fluoro-benzaldehyde (in DMSO)	DMSO		J. Am. Chem. Soc. 2011, 133, 8240-8251 DOI: 10.1021/ja200820m
3-methoxy-benzaldehyde (in DMSO)	DMSO		J. Am. Chem. Soc. 2011, 133, 8240-8251 DOI: 10.1021/ja200820m
4-fluoro-benzaldehyde (in DMSO)	DMSO		J. Am. Chem. Soc. 2011, 133, 8240-8251 DOI: 10.1021/ja200820m
hexanal (in DMSO)	DMSO		J. Am. Chem. Soc. 2011, 133, 8240-8251 DOI: 10.1021/ja200820m
butanal (in DMSO)	DMSO		J. Am. Chem. Soc. 2011, 133, 8240-8251 DOI: 10.1021/ja200820m
cinnamaldehyde (in DMSO)	DMSO		J. Am. Chem. Soc. 2011, 133, 8240-8251 DOI: 10.1021/ja200820m
p-nitro-cinnamaldehyde (in DMSO)	DMSO		J. Am. Chem. Soc. 2011, 133, 8240-8251 DOI: 10.1021/ja200820m
(E)-N-benzylidene-4-methylbenzenesulfonamide (in DMSO)	DMSO	E Parameter: -11.50	J. Am. Chem. Soc. 2011, 133, 8240-8251 DOI: 10.1021/ja200820m
(E)-N-(4-methoxybenzylidene)-4-methylbenzenesulfonamide (in DMSO)	DMSO	E Parameter: -13.05	J. Am. Chem. Soc. 2011, 133, 8240-8251 DOI: 10.1021/ja200820m
(E)-N-(4-(dimethylamino)benzylidene)-4-methylbenzenesulfonamide (in DMSO)	DMSO	E Parameter: -15.09	J. Am. Chem. Soc. 2011, 133, 8240-8251 DOI: 10.1021/ja200820m
(E)-tert-butyl benzylidenecarbamate (in DMSO)	DMSO	E Parameter: -14.22	J. Am. Chem. Soc. 2011, 133, 8240-8251 DOI: 10.1021/ja200820m
(E)-N-benzylidene-P,P-diphenylphosphinic amide	DMSO	E Parameter: -15.89	J. Am. Chem. Soc. 2011, 133, 8240-8251 DOI: 10.1021/ja200820m
(4-F)-tritylium ion		E Parameter: 0.35	Eur. J. Org. Chem. 2011, , 6470-6475 DOI: 10.1002/ejoc.201100910
(4-F)2-tritylium ion		E Parameter: 0.17	Eur. J. Org. Chem. 2011, , 6470-6475 DOI: 10.1002/ejoc.201100910
(4-F)3-tritylium ion		E Parameter: 0.05	Eur. J. Org. Chem. 2011, , 6470-6475 DOI: 10.1002/ejoc.201100910
(3-F)-tritylium ion		E Parameter: 1.01	Eur. J. Org. Chem. 2011, , 6470-6475 DOI: 10.1002/ejoc.201100910
(3-F)2-tritylium ion		E Parameter: 1.54	Eur. J. Org. Chem. 2011, , 6470-6475 DOI: 10.1002/ejoc.201100910
(3-F)3-tritylium ion		E Parameter: 2.07	Eur. J. Org. Chem. 2011, , 6470-6475 DOI: 10.1002/ejoc.201100910
(3-F)4-tritylium ion		E Parameter: 2.54	Eur. J. Org. Chem. 2011, , 6470-6475 DOI: 10.1002/ejoc.201100910
diarylallylium ion (3,3-F2)2		E Parameter: 6.11	J. Org. Chem. 2011, 76, 9391-9408 DOI: 10.1021/jo201668w
diarylallylium ion (3-F)2		E Parameter: 4.15	J. Org. Chem. 2011, 76, 9391-9408 DOI: 10.1021/jo201668w
diarylallylium ion (4-Br)2		E Parameter: 2.85	J. Org. Chem. 2011, 76, 9391-9408 DOI: 10.1021/jo201668w
diarylallylium ion (4-Cl)2		E Parameter: 2.69	J. Org. Chem. 2011, 76, 9391-9408 DOI: 10.1021/jo201668w
diphenylallylium ion		E Parameter: 2.70	J. Org. Chem. 2011, 76, 9391-9408 DOI: 10.1021/jo201668w
di-p-tolyl-allylium ion		E Parameter: 1.23	J. Org. Chem. 2011, 76, 9391-9408 DOI: 10.1021/jo201668w
di-p-anisyl-allylium ion		E Parameter: -1.45	J. Org. Chem. 2011, 76, 9391-9408 DOI: 10.1021/jo201668w
diarylallylium ion (4-NMe2)2		E Parameter: -7.50	J. Org. Chem. 2011, 76, 9391-9408 DOI: 10.1021/jo201668w
bis(julidin-9-yl)allylium ion		E Parameter: -9.78	J. Org. Chem. 2011, 76, 9391-9408 DOI: 10.1021/jo201668w
4-methoxy-<i>trans-beta</i>-nitrostyrene		E Parameter: -14.70	J. Org. Chem. 2011, 76, 9370-9378 DOI: 10.1021/jo201678u
4-methyl-<i>trans-beta</i>-nitrostyrene		E Parameter: -14.23	J. Org. Chem. 2011, 76, 9370-9378 DOI: 10.1021/jo201678u
<i>trans-beta</i>-nitrostyrene		E Parameter: -13.85	J. Org. Chem. 2011, 76, 9370-9378 DOI: 10.1021/jo201678u
4-bromo-<i>trans-beta</i>-nitrostyrene		E Parameter: -13.37	J. Org. Chem. 2011, 76, 9370-9378 DOI: 10.1021/jo201678u
4-cyano-<i>trans-beta</i>-nitrostyrene		E Parameter: -12.61	J. Org. Chem. 2011, 76, 9370-9378 DOI: 10.1021/jo201678u
4-nitro-<i>trans-beta</i>-nitrostyrene		E Parameter: -12.37	J. Org. Chem. 2011, 76, 9370-9378 DOI: 10.1021/jo201678u
MacMillan-iminium ion (2nd generation)	MeCN	E Parameter: -5.52	Angew. Chem. Int. Ed. 2011, 50, 9953-9956 DOI: 10.1002/anie.201103683
MacMillan-iminium ion (spiro)	MeCN	E Parameter: -7.67	Angew. Chem. Int. Ed. 2011, 50, 9953-9956 DOI: 10.1002/anie.201103683
bh6a		E Parameter: -18.60	Chem. Eur. J. 2010, 16, 1365-1371 DOI: 10.1002/chem.200902487
bh 6f		E Parameter: -18.90	Chem. Eur. J. 2010, 16, 1365-1371 DOI: 10.1002/chem.200902487
bh 6i		E Parameter: -19.10	Chem. Eur. J. 2010, 16, 1365-1371 DOI: 10.1002/chem.200902487
bh6j		E Parameter: -17.90	Chem. Eur. J. 2010, 16, 1365-1371 DOI: 10.1002/chem.200902487
bh 6k		E Parameter: -18.20	Chem. Eur. J. 2010, 16, 1365-1371 DOI: 10.1002/chem.200902487
bh 6l		E Parameter: -18.90	Chem. Eur. J. 2010, 16, 1365-1371 DOI: 10.1002/chem.200902487
bh 6m		E Parameter: -17.30	Chem. Eur. J. 2010, 16, 1365-1371 DOI: 10.1002/chem.200902487
cumyl cation		E Parameter: 5.74	Macromolecules 2010, 43, 1719-1723 DOI: 10.1021/ma9024569
1,2-diaza-1,3-diene 1a	DMSO	E Parameter: -13.28	Chem. Eur. J. 2010, 16, 12008-12016 DOI: 10.1002/chem.201000828
1,2-diaza-1,3-diene 1b	DMSO	E Parameter: -13.90	Chem. Eur. J. 2010, 16, 12008-12016 DOI: 10.1002/chem.201000828
1,2-diaza-1,3-diene 1c	DMSO	E Parameter: -14.91	Chem. Eur. J. 2010, 16, 12008-12016 DOI: 10.1002/chem.201000828
1,2-diaza-1,3-diene 1d	DMSO	E Parameter: -15.38	Chem. Eur. J. 2010, 16, 12008-12016 DOI: 10.1002/chem.201000828
1,2-diaza-1,3-diene 1e	MeOH	E Parameter: -14.90	Chem. Eur. J. 2010, 16, 12008-12016 DOI: 10.1002/chem.201000828
1,2-diaza-1,3-diene 1f	MeOH	E Parameter: -15.30	Chem. Eur. J. 2010, 16, 12008-12016 DOI: 10.1002/chem.201000828
2,3,4,5,6,6-hexachlorocyclohexa-2,4-dien-1-one	MeCN	E Parameter: -6.75	Org. Lett. 2010, 12, 2238-2241 DOI: 10.1021/ol100592j
5,7,7-trichloro-8(7H)-quinolinone	MeCN	E Parameter: -10.48	Org. Lett. 2010, 12, 2238-2241 DOI: 10.1021/ol100592j
2,2,4-trichloro-1(2H)-naphthalenone	MeCN	E Parameter: -11.24	Org. Lett. 2010, 12, 2238-2241 DOI: 10.1021/ol100592j
dibenzyl azodicarboxylate	MeCN	E Parameter: -8.89	Chem. Eur. J. 2010, 16, 11670-11677 DOI: 10.1002/chem.201001598
diethyl azodicarboxylate	MeCN	E Parameter: -10.15	Chem. Eur. J. 2010, 16, 11670-11677 DOI: 10.1002/chem.201001598
diisopropyl azodicarboxylate	MeCN	E Parameter: -10.71	Chem. Eur. J. 2010, 16, 11670-11677 DOI: 10.1002/chem.201001598
di-tert-butyl azodicarboxylate	MeCN	E Parameter: -12.23	Chem. Eur. J. 2010, 16, 11670-11677 DOI: 10.1002/chem.201001598
2,6-diphenyl-4-benzylidenecyclohexa-2,5-dienone	0	E Parameter: -11.87	Eur. J. Org. Chem. 2009, , 3203-3211 DOI: 10.1002/ejoc.200900299
2,6-dimethoxy-4-(4-methoxybenzylidene)cyclohexa-2,5-dienone	0	E Parameter: -16.38	Eur. J. Org. Chem. 2009, , 3203-3211 DOI: 10.1002/ejoc.200900299
2,6-dimethoxy-4-(4-(dimethylamino)benzylidene)cyclohexa-2,5-dienone	0	E Parameter: -17.18	Eur. J. Org. Chem. 2009, , 3203-3211 DOI: 10.1002/ejoc.200900299
2,6-dimethyl-4-(4-(dimethylamino)benzylidene)cyclohexa-2,5-dienone	0	E Parameter: -16.36	Eur. J. Org. Chem. 2009, , 3203-3211 DOI: 10.1002/ejoc.200900299
2,6-di-tert.butyl-4-(3-fluorobenzylidene)cyclohexa-2,5-dienone	0	E Parameter: -15.03	Eur. J. Org. Chem. 2009, , 3203-3211 DOI: 10.1002/ejoc.200900299
2,6-di-tert.butyl-4-(3,5-difluorobenzylidene)cyclohexa-2,5-dienone	0	E Parameter: -14.50	Eur. J. Org. Chem. 2009, , 3203-3211 DOI: 10.1002/ejoc.200900299
2,6-di-tert.butyl-4-(4-nitrobenzylidene)cyclohexa-2,5-dienone	0	E Parameter: -14.36	Eur. J. Org. Chem. 2009, , 3203-3211 DOI: 10.1002/ejoc.200900299
indolecarboxylate derived iminium ion	dichloromethane	E Parameter: -9.50	Angew. Chem. Int. Ed. 2009, 48, 5034-5037 DOI: 10.1002/anie.200900933
benzylidene-Meldrum's acid	0	E Parameter: -9.15	J. Org. Chem. 2008, 73, 2738-2745 DOI: 10.1021/jo702590s
p-(methoxy)benzylidene Meldrum's acid	0	E Parameter: -10.28	J. Org. Chem. 2008, 73, 2738-2745 DOI: 10.1021/jo702590s
p-(dimethylamino)benzylidene Meldrum's acid	0	E Parameter: -12.76	J. Org. Chem. 2008, 73, 2738-2745 DOI: 10.1021/jo702590s
jul Meldrum's acid	0	E Parameter: -13.97	J. Org. Chem. 2008, 73, 2738-2745 DOI: 10.1021/jo702590s
diethyl benzylidene malonate	0	E Parameter: -20.55	Chem. Eur. J. 2008, 14, 9675-9682 DOI: 10.1002/chem.200801277
diethyl 4-nitrobenzylidene malonate	0	E Parameter: -17.67	Chem. Eur. J. 2008, 14, 9675-9682 DOI: 10.1002/chem.200801277
diethyl 4-cyano-benzylidene malonate	0	E Parameter: -18.06	Chem. Eur. J. 2008, 14, 9675-9682 DOI: 10.1002/chem.200801277
diethyl 3-chloro-benzylidene malonate	0	E Parameter: -18.98	Chem. Eur. J. 2008, 14, 9675-9682 DOI: 10.1002/chem.200801277
diethyl 4-methyl-benzylidene malonate	0	E Parameter: -21.11	Chem. Eur. J. 2008, 14, 9675-9682 DOI: 10.1002/chem.200801277
diethyl 4-methoxy-benzylidene malonate	0	E Parameter: -21.47	Chem. Eur. J. 2008, 14, 9675-9682 DOI: 10.1002/chem.200801277
diethyl 4-(dimethylamino)benzylidene malonate	0	E Parameter: -23.10	Chem. Eur. J. 2008, 14, 9675-9682 DOI: 10.1002/chem.200801277
diethyl 2-((1-methyl-1,2,3,4-tetrahydroquinolin-6-yl)methylene)malonate	0	E Parameter: -23.40	Chem. Eur. J. 2008, 14, 9675-9682 DOI: 10.1002/chem.200801277
diethyl 2-((julolidine-9-yl)methylene)malonate	0	E Parameter: -23.80	Chem. Eur. J. 2008, 14, 9675-9682 DOI: 10.1002/chem.200801277
Me2N+=CH-CH-Ph	0	E Parameter: -9.20	Angew. Chem. Int. Ed. 2008, 47, 8723-8726 DOI: 10.1002/anie.200802889
pyrN+=CH-CH-Ph	0	E Parameter: -9.80	Angew. Chem. Int. Ed. 2008, 47, 8723-8726 DOI: 10.1002/anie.200802889
pipN+=CH-CH-Ph	0	E Parameter: -10.30	Angew. Chem. Int. Ed. 2008, 47, 8723-8726 DOI: 10.1002/anie.200802889
(PhCH2)2N+=CH-CH-Ph	0	E Parameter: -8.50	Angew. Chem. Int. Ed. 2008, 47, 8723-8726 DOI: 10.1002/anie.200802889
Jorgensen/Hayashi-iminium ion	0	E Parameter: -8.20	Angew. Chem. Int. Ed. 2008, 47, 8723-8726 DOI: 10.1002/anie.200802889
mor iminium	0	E Parameter: -8.60	Angew. Chem. Int. Ed. 2008, 47, 8723-8726 DOI: 10.1002/anie.200802889
2-(p-(dimethylamino)benzylidene)-indan-1,3-dione	0	E Parameter: -13.56	Org. Biomol. Chem. 2007, 5, 3020-3026 DOI: 10.1039/b708025e
2-(p-methoxybenzylidene)-indan-1,3-dione	0	E Parameter: -11.32	Org. Biomol. Chem. 2007, 5, 3020-3026 DOI: 10.1039/b708025e
2-benzylidene-indan-1,3-dione	0	E Parameter: -10.11	Org. Biomol. Chem. 2007, 5, 3020-3026 DOI: 10.1039/b708025e
jul-indan-1,3-dione	0	E Parameter: -14.68	Org. Biomol. Chem. 2007, 5, 3020-3026 DOI: 10.1039/b708025e
aniBBS	0	E Parameter: -10.37	J. Org. Chem. 2007, 72, 9170-9180 DOI: 10.1021/jo071273g
dmaBBS	0	E Parameter: -12.76	J. Org. Chem. 2007, 72, 9170-9180 DOI: 10.1021/jo071273g
julBBS	0	E Parameter: -13.84	J. Org. Chem. 2007, 72, 9170-9180 DOI: 10.1021/jo071273g
dma(S)BBS	0	E Parameter: -10.73	J. Org. Chem. 2007, 72, 9170-9180 DOI: 10.1021/jo071273g
jul(S)BBS	0	E Parameter: -11.89	J. Org. Chem. 2007, 72, 9170-9180 DOI: 10.1021/jo071273g
4-nitrobenzodifuroxan (NBDF)	0	E Parameter: -6.15	Chem. Eur. J. 2007, 13, 8317-8324 DOI: 10.1002/chem.200700676
4,6-dinitrobenzofuroxan	0	E Parameter: -5.06	J. Org. Chem. 2006, 71, 9088-9095 DOI: 10.1021/jo0614339
1,3,5-trinitrobenzene	0	E Parameter: -13.19	J. Org. Chem. 2005, 70, 6242-6253 DOI: 10.1021/jo0505526
6-nitro-tetrazolo[1,5a]pyridine	0	E Parameter: -9.05	J. Org. Chem. 2005, 70, 6242-6253 DOI: 10.1021/jo0505526
dicarbonyl(cyclopentadienyl)propene-iron(II)		E Parameter: -11.20	Helv. Chim. Acta 2005, 88, 1754-1768 DOI: 10.1002/hlca.200590137
4-nitro-6-(trifluoromethylsulfonyl)benzofuroxan	0	E Parameter: -4.91	J. Org. Chem. 2005, 70, 6242-6253 DOI: 10.1021/jo0505526
4,6-dinitrotetrazolopyridine	0	E Parameter: -4.67	J. Org. Chem. 2005, 70, 6242-6253 DOI: 10.1021/jo0505526
4,6-dinitrobenzofurazan	0	E Parameter: -5.46	J. Org. Chem. 2005, 70, 6242-6253 DOI: 10.1021/jo0505526
2,4-dinitrothiophene	0	E Parameter: -12.33	J. Org. Chem. 2005, 70, 6242-6253 DOI: 10.1021/jo0505526
6-cyano-4-nitrobenzofuroxan	0	E Parameter: -7.01	J. Org. Chem. 2005, 70, 6242-6253 DOI: 10.1021/jo0505526
4-cyano-6-nitro-benzofuroxane	0	E Parameter: -6.41	J. Org. Chem. 2005, 70, 6242-6253 DOI: 10.1021/jo0505526
4-aza-6-nitrobenzofuroxan	0	E Parameter: -5.86	J. Org. Chem. 2005, 70, 6242-6253 DOI: 10.1021/jo0505526
(2,4,6-trimethylphenyl)ethylium ion	0	E Parameter: 6.04	Macromolecules 2005, 38, 33-40 DOI: 10.1021/ma048389o
1,3-bis(2,4,6-trimethylphenyl)but-1-ylium ion	0	E Parameter: 6.16	Macromolecules 2005, 38, 33-40 DOI: 10.1021/ma048389o
5-methoxyfuroxano[3,4-d]pyrimidine	0	E Parameter: -8.37	J. Phys. Org. Chem. 2003, 16, 431-437 DOI: 10.1002/poc.606
benzylidenemalononitrile	0	E Parameter: -9.42	J. Org. Chem. 2003, 68, 6880-6886 DOI: 10.1021/jo0344182
p-(methoxy)benzylidenemalononitrile	0	E Parameter: -10.80	J. Org. Chem. 2003, 68, 6880-6886 DOI: 10.1021/jo0344182
p-(dimethylamino)benzylidenemalononitrile	0	E Parameter: -13.30	J. Org. Chem. 2003, 68, 6880-6886 DOI: 10.1021/jo0344182
pop(tol)CH+	0	E Parameter: 2.16	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
fc(ani)CH+	0	E Parameter: -2.90	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
fc(Me)CH+	0	E Parameter: -2.57	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
fc2CH+	0	E Parameter: -8.54	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
C7H7+-Fe(CO)3		E Parameter: -3.49	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
C7H9+-Fe(CO)3		E Parameter: -9.21	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
C6H7+-Fe(CO)3		E Parameter: -7.76	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
C6H6OMe+-Fe(CO)3		E Parameter: -8.94	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
benzaldehyde-boron trichloride complex		E Parameter: 1.12	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
4-chlorobenzaldehyde-boron trichloride complex		E Parameter: 1.44	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
tropylium ion	0	E Parameter: -3.72	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
propyn-1-ylium-Co2(CO)6		E Parameter: -0.84	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
1-phenyl-proyn-ylium-Co2(CO)6		E Parameter: -0.97	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
3-phenylpropyn-1-ylium-Co2(CO)6		E Parameter: -1.58	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
3-(trimethylsilyl)propyn-1-ylium-Co2(CO)6		E Parameter: -1.60	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
1-phenyl-propyn-1-ylium-Co2(CO)5(PPh3)		E Parameter: -6.19	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
2-phenyl-1,3-dithiolan-2-ylium ion	0	E Parameter: -5.91	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
2-phenyl-1,3-dithianylium ion	0	E Parameter: -6.43	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
1,3-dithianylium ion	0	E Parameter: -2.14	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
N-ethylidenecarbazolium ion	0	E Parameter: 2.41	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
N-methylacridinium ion	0	E Parameter: -7.15	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
dimethylmethyleneammonium ion	0	E Parameter: -6.69	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
methyl(phenyl)methyleneammonium ion	0	E Parameter: -5.17	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
Vilsmeier ion	0	E Parameter: -5.77	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
methoxy-phenylmethylium ion	0	E Parameter: 2.97	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
methoxy-(4-methoxyphenyl)methylium ion	0	E Parameter: 0.14	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
methoxy-(4-methylphenyl)methylium ion	0	E Parameter: 1.90	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
Pd-allyl cation		E Parameter: -10.11	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
flavylium ion	0	E Parameter: -3.45	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
2-(4-methoxyphenyl)chromenylium ion	0	E Parameter: -4.95	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
1,1,3-triphenylallylium ion	0	E Parameter: 0.98	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
1,1-dianisyl-3-phenylallylium ion	0	E Parameter: -2.67	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
1,1-bis(4-dimethylaminophenyl)-3-phenylallylium ion	0	E Parameter: -8.97	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
1,1,3-tris(4-(dimethylamino)phenyl)allylium ion	0	E Parameter: -9.84	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
1-phenylcyclopent-2-enylium ion	0	E Parameter: 2.89	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
1-(4-chlorophenyl)cyclopent-2-enylium ion	0	E Parameter: 3.20	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
1,3-diphenylpropyn-1-ylium-Cr(CO)3		E Parameter: 1.07	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
1,1,3-triphenylpropyn-1-ylium-Cr(CO)3		E Parameter: -0.25	Acc. Chem. Res. 2003, 36, 66-77 DOI: 10.1021/ar020094c
tritylium ion (Ph3C+)	0	E Parameter: 0.51	J. Am. Chem. Soc. 2003, 125, 286-295 DOI: 10.1021/ja021010y
(4-CF3)2-tritylium ion		E Parameter: 2.28	J. Am. Chem. Soc. 2003, 125, 286-295 DOI: 10.1021/ja021010y
(3-Cl)3-tritylium ion		E Parameter: 1.99	J. Am. Chem. Soc. 2003, 125, 286-295 DOI: 10.1021/ja021010y
(4-CF3)-tritylium ion		E Parameter: 1.33	J. Am. Chem. Soc. 2003, 125, 286-295 DOI: 10.1021/ja021010y
(3-Cl)-tritylium ion		E Parameter: 1.06	J. Am. Chem. Soc. 2003, 125, 286-295 DOI: 10.1021/ja021010y
(3-CF3)-tritylium ion		E Parameter: 1.18	J. Am. Chem. Soc. 2003, 125, 286-295 DOI: 10.1021/ja021010y
(4-Me)-tritylium ion		E Parameter: -0.13	J. Am. Chem. Soc. 2003, 125, 286-295 DOI: 10.1021/ja021010y
(4-Me)2-tritylium ion		E Parameter: -0.70	J. Am. Chem. Soc. 2003, 125, 286-295 DOI: 10.1021/ja021010y
(4-Me)3-tritylium ion		E Parameter: -1.21	J. Am. Chem. Soc. 2003, 125, 286-295 DOI: 10.1021/ja021010y
(4-MeO,3-OMe)-tritylium ion		E Parameter: -1.62	J. Am. Chem. Soc. 2003, 125, 286-295 DOI: 10.1021/ja021010y
(4-OMe,3-Me)-tritylium ion		E Parameter: -1.84	J. Am. Chem. Soc. 2003, 125, 286-295 DOI: 10.1021/ja021010y
(4-MeO,4-Me)-tritylium ion		E Parameter: -2.13	J. Am. Chem. Soc. 2003, 125, 286-295 DOI: 10.1021/ja021010y
(4-MeO)2-tritylium ion		E Parameter: -3.04	J. Am. Chem. Soc. 2003, 125, 286-295 DOI: 10.1021/ja021010y
(4-MeO)3-tritylium ion		E Parameter: -4.35	J. Am. Chem. Soc. 2003, 125, 286-295 DOI: 10.1021/ja021010y
(4-NMe2)-tritylium ion		E Parameter: -7.93	J. Am. Chem. Soc. 2003, 125, 286-295 DOI: 10.1021/ja021010y
(4-NMe2)2-tritylium ion (= Malachite green)		E Parameter: -10.29	J. Am. Chem. Soc. 2003, 125, 286-295 DOI: 10.1021/ja021010y
(4-NMe2)3-tritylium ion (= Crystal violet)		E Parameter: -11.26	J. Am. Chem. Soc. 2003, 125, 286-295 DOI: 10.1021/ja021010y
ani(Br)2QM	0	E Parameter: -8.63	Angew. Chem. Int. Ed. 2002, 41, 91-95 DOI: 10.1002/1521-3773(20020104)41:1<91::AID-ANIE91>3.0.CO;2-P
ani(Ph)2QM	0	E Parameter: -12.18	Angew. Chem. Int. Ed. 2002, 41, 91-95 DOI: 10.1002/1521-3773(20020104)41:1<91::AID-ANIE91>3.0.CO;2-P
dma(Ph)2QM	0	E Parameter: -13.39	Angew. Chem. Int. Ed. 2002, 41, 91-95 DOI: 10.1002/1521-3773(20020104)41:1<91::AID-ANIE91>3.0.CO;2-P
tol(t-Bu)2QM	0	E Parameter: -15.83	Angew. Chem. Int. Ed. 2002, 41, 91-95 DOI: 10.1002/1521-3773(20020104)41:1<91::AID-ANIE91>3.0.CO;2-P
ani(t-Bu)2QM		E Parameter: -16.11	Angew. Chem. Int. Ed. 2002, 41, 91-95 DOI: 10.1002/1521-3773(20020104)41:1<91::AID-ANIE91>3.0.CO;2-P
dma(t-Bu)2QM		E Parameter: -17.29	Angew. Chem. Int. Ed. 2002, 41, 91-95 DOI: 10.1002/1521-3773(20020104)41:1<91::AID-ANIE91>3.0.CO;2-P
jul(t-Bu)2QM	0	E Parameter: -17.90	Angew. Chem. Int. Ed. 2002, 41, 91-95 DOI: 10.1002/1521-3773(20020104)41:1<91::AID-ANIE91>3.0.CO;2-P
(fur)2CH+	0	E Parameter: -1.36	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
(ani)2CH+	0	E Parameter: 0.00	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
(tol)2CH+	0	E Parameter: 3.63	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
(pfa)2CH+	0	E Parameter: -3.14	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
(mfa)2CH+	0	E Parameter: -3.85	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
(dpa)2CH+	0	E Parameter: -4.72	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
(mor)2CH+	0	E Parameter: -5.53	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
(mpa)2CH+	0	E Parameter: -5.89	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
(dma)2CH+	0	E Parameter: -7.02	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
(pyr)2CH+	0	E Parameter: -7.69	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
(thq)2CH+	0	E Parameter: -8.22	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
(ind)2CH+	0	E Parameter: -8.76	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
(jul)2CH+	0	E Parameter: -9.45	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
(lil)2CH+	0	E Parameter: -10.04	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
ani(pop)CH+	0	E Parameter: 0.61	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
ani(Ph)CH+	0	E Parameter: 2.11	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
ani(tol)CH+	0	E Parameter: 1.48	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
pop(Ph)CH+	0	E Parameter: 2.90	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
fc(Ph)CH+	0	E Parameter: -2.64	J. Am. Chem. Soc. 2001, 123, 9500-9512 DOI: 10.1021/ja010890y
dibenzo[a,d]tropylium ion	dichloromethane	E Parameter: -0.63	Liebigs Ann. 1995, , 2005-2009 DOI: 10.1002/jlac.1995199511281