Mayr's Database Of Reactivity Parameters
AK Prof. Mayr

Acceptor-Substituted Ethylenes

For reactivities of structurally related compounds go to: Electrophiles » C-Electrophiles
Found 125 Molecules.
Molecule Solvent Reactivity Parameters Classification Reference (sort by title or year)
image of molecule

tol(t-Bu)2QM		0E 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
image of molecule

tert-butyl prop-2-enoate (in DMSO)		DMSOE Parameter: -20.22
***J. Am. Chem. Soc. 2017, 139, 13318-13329
DOI: 10.1021/jacs.7b05106
image of molecule

p-(methoxy)benzylidenemalononitrile		0E Parameter: -10.80
***J. Org. Chem. 2003, 68, 6880-6886
DOI: 10.1021/jo0344182
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p-(methoxy)benzylidene Meldrum's acid		0E Parameter: -10.28
***J. Org. Chem. 2008, 73, 2738-2745
DOI: 10.1021/jo702590s
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p-(dimethylamino)benzylidenemalononitrile		0E Parameter: -13.30
***J. Org. Chem. 2003, 68, 6880-6886
DOI: 10.1021/jo0344182
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p-(dimethylamino)benzylidene Meldrum's acid		0E Parameter: -12.76
***J. Org. Chem. 2008, 73, 2738-2745
DOI: 10.1021/jo702590s
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N-methyl maleimide		DMSOE Parameter: -14.07
***Eur. J. Org. Chem. 2014, , 2956-2963
DOI: 10.1002/ejoc.201301779
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N,N-dimethylprop-2-enamide (in DMSO)		DMSOE Parameter: -23.54
***J. Am. Chem. Soc. 2017, 139, 13318-13329
DOI: 10.1021/jacs.7b05106
image of molecule

methyl prop-2-enoate (in DMSO)		DMSOE Parameter: -18.84
***J. Am. Chem. Soc. 2017, 139, 13318-13329
DOI: 10.1021/jacs.7b05106
image of molecule

maleic anhydride		DMSOE Parameter: -11.31
***Eur. J. Org. Chem. 2014, , 2956-2963
DOI: 10.1002/ejoc.201301779
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julBBS		0E Parameter: -13.84
***J. Org. Chem. 2007, 72, 9170-9180
DOI: 10.1021/jo071273g
image of molecule

jul-indan-1,3-dione		0E Parameter: -14.68
***Org. Biomol. Chem. 2007, 5, 3020-3026
DOI: 10.1039/b708025e
image of molecule

jul(t-Bu)2QM		0E 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
image of molecule

jul(S)BBS		0E Parameter: -11.89
***J. Org. Chem. 2007, 72, 9170-9180
DOI: 10.1021/jo071273g
image of molecule

jul Meldrum's acid		0E Parameter: -13.97
***J. Org. Chem. 2008, 73, 2738-2745
DOI: 10.1021/jo702590s
image of molecule

hex-3-yn-2-one		0E Parameter: -17.90
-Angew. Chem. Int. Ed. 2019, 58, 17704-17708
DOI: 10.1002/anie.201909803
image of molecule

furan-2(5H)-one		DMSOE Parameter: -20.70
***Chem. Sci. 2021, 12, 4850-4865
DOI: 10.1039/D0SC06628A
image of molecule

fumaronitrile		DMSOE Parameter: -15.71
***Eur. J. Org. Chem. 2014, , 2956-2963
DOI: 10.1002/ejoc.201301779
image of molecule

ethyl prop-2-enoate (in DMSO)		DMSOE Parameter: -19.07
***J. Am. Chem. Soc. 2017, 139, 13318-13329
DOI: 10.1021/jacs.7b05106
image of molecule

ethyl cinnamate (in DMSO)		DMSOE Parameter: -24.52
**J. Am. Chem. Soc. 2017, 139, 13318-13329
DOI: 10.1021/jacs.7b05106
image of molecule

ethyl 2-methylprop-2-enoate (in DMSO)		DMSOE Parameter: -22.77
**J. Am. Chem. Soc. 2017, 139, 13318-13329
DOI: 10.1021/jacs.7b05106
image of molecule

ethyl (E)-but-2-enoate (in DMSO)		DMSOE Parameter: -23.59
**J. Am. Chem. Soc. 2017, 139, 13318-13329
DOI: 10.1021/jacs.7b05106
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ethenylsulfonylbenzene (in DMSO)		DMSOE Parameter: -18.36
***J. Am. Chem. Soc. 2017, 139, 13318-13329
DOI: 10.1021/jacs.7b05106
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ethenesulfonyl fluoride (ESF)		DMSOE Parameter: -12.09
***Angew. Chem. Int. Ed. 2016, 55, 12664-12667
DOI: 10.1002/anie.201601875
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E)-2,6-di-tert-butyl-4-(3-(4-chlorophenyl)allylidene)cyclohexa-2,5-dien-1-one		DMSOE Parameter: -16.84
***Org. Lett. 2020, 22, 2182-2186
DOI: 10.1021/acs.orglett.0c00338
image of molecule

dmaBBS		0E Parameter: -12.76
***J. Org. Chem. 2007, 72, 9170-9180
DOI: 10.1021/jo071273g
image of molecule

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
image of molecule

dma(S)BBS		0E Parameter: -10.73
***J. Org. Chem. 2007, 72, 9170-9180
DOI: 10.1021/jo071273g
image of molecule

dma(Ph)2QM		0E 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
image of molecule

dihydro-2H-pyran-2-one		DMSOE Parameter: -21.80
**Chem. Sci. 2021, 12, 4850-4865
DOI: 10.1039/D0SC06628A
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diethyl maleate		DMSOE Parameter: -19.49
***Eur. J. Org. Chem. 2014, , 2956-2963
DOI: 10.1002/ejoc.201301779
image of molecule

diethyl fumarate		DMSOE Parameter: -17.79
***Eur. J. Org. Chem. 2014, , 2956-2963
DOI: 10.1002/ejoc.201301779
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diethyl benzylidene malonate		0E Parameter: -20.55
***Chem. Eur. J. 2008, 14, 9675-9682
DOI: 10.1002/chem.200801277
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diethyl 4-nitrobenzylidene malonate		0E Parameter: -17.67
***Chem. Eur. J. 2008, 14, 9675-9682
DOI: 10.1002/chem.200801277
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diethyl 4-methyl-benzylidene malonate		0E Parameter: -21.11
***Chem. Eur. J. 2008, 14, 9675-9682
DOI: 10.1002/chem.200801277
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diethyl 4-methoxy-benzylidene malonate		0E Parameter: -21.47
***Chem. Eur. J. 2008, 14, 9675-9682
DOI: 10.1002/chem.200801277
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diethyl 4-cyano-benzylidene malonate		0E Parameter: -18.06
***Chem. Eur. J. 2008, 14, 9675-9682
DOI: 10.1002/chem.200801277
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diethyl 4-(dimethylamino)benzylidene malonate		0E Parameter: -23.10
***Chem. Eur. J. 2008, 14, 9675-9682
DOI: 10.1002/chem.200801277
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diethyl 3-chloro-benzylidene malonate		0E Parameter: -18.98
***Chem. Eur. J. 2008, 14, 9675-9682
DOI: 10.1002/chem.200801277
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diethyl 2-((julolidine-9-yl)methylene)malonate		0E Parameter: -23.80
*Chem. Eur. J. 2008, 14, 9675-9682
DOI: 10.1002/chem.200801277
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diethyl 2-((1-methyl-1,2,3,4-tetrahydroquinolin-6-yl)methylene)malonate		0E Parameter: -23.40
*Chem. Eur. J. 2008, 14, 9675-9682
DOI: 10.1002/chem.200801277
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cyclopentenone		DMSOE Parameter: -20.60
***Chem. Sci. 2021, 12, 4850-4865
DOI: 10.1039/D0SC06628A
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cyclohexenone		DMSOE Parameter: -22.10
***Chem. Sci. 2021, 12, 4850-4865
DOI: 10.1039/D0SC06628A
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cycloheptenone		DMSOE Parameter: -22.00
***Chem. Sci. 2021, 12, 4850-4865
DOI: 10.1039/D0SC06628A
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cinnamonitrile (in DMSO)		DMSOE Parameter: -24.60
*J. Am. Chem. Soc. 2017, 139, 13318-13329
DOI: 10.1021/jacs.7b05106
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butynone		0E Parameter: -16.60
-Angew. Chem. Int. Ed. 2019, 58, 17704-17708
DOI: 10.1002/anie.201909803
image of molecule

but-3-en-2-one (in DMSO)		DMSOE Parameter: -16.76
***J. Am. Chem. Soc. 2017, 139, 13318-13329
DOI: 10.1021/jacs.7b05106
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bh6j		E Parameter: -17.90
**Chem. Eur. J. 2010, 16, 1365-1371
DOI: 10.1002/chem.200902487
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bh6a		E Parameter: -18.60
**Chem. Eur. J. 2010, 16, 1365-1371
DOI: 10.1002/chem.200902487
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bh 6m		E Parameter: -17.30
*Chem. Eur. J. 2010, 16, 1365-1371
DOI: 10.1002/chem.200902487
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bh 6l		E Parameter: -18.90
*Chem. Eur. J. 2010, 16, 1365-1371
DOI: 10.1002/chem.200902487
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bh 6k		E Parameter: -18.20
*Chem. Eur. J. 2010, 16, 1365-1371
DOI: 10.1002/chem.200902487
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bh 6i		E Parameter: -19.10
**Chem. Eur. J. 2010, 16, 1365-1371
DOI: 10.1002/chem.200902487
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bh 6f		E Parameter: -18.90
**Chem. Eur. J. 2010, 16, 1365-1371
DOI: 10.1002/chem.200902487
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benzylidenemalononitrile		0E Parameter: -9.42
***J. Org. Chem. 2003, 68, 6880-6886
DOI: 10.1021/jo0344182
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benzylidene-Meldrum's acid		0E Parameter: -9.15
***J. Org. Chem. 2008, 73, 2738-2745
DOI: 10.1021/jo702590s
image of molecule

aniBBS		0E Parameter: -10.37
***J. Org. Chem. 2007, 72, 9170-9180
DOI: 10.1021/jo071273g
image of molecule

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
image of molecule

ani(Ph)2QM		0E 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
image of molecule

ani(Br)2QM		0E 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
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acrylonitrile (in DMSO)		DMSOE Parameter: -19.05
***J. Am. Chem. Soc. 2017, 139, 13318-13329
DOI: 10.1021/jacs.7b05106
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<i>trans-beta</i>-nitrostyrene		E Parameter: -13.85
***J. Org. Chem. 2011, 76, 9370-9378
DOI: 10.1021/jo201678u
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4-phenylbut-3-yn-2-one		0E Parameter: -16.90
-Angew. Chem. Int. Ed. 2019, 58, 17704-17708
DOI: 10.1002/anie.201909803
image of molecule

4-nitro-<i>trans-beta</i>-nitrostyrene		E Parameter: -12.37
***J. Org. Chem. 2011, 76, 9370-9378
DOI: 10.1021/jo201678u
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4-methyl-<i>trans-beta</i>-nitrostyrene		E Parameter: -14.23
***J. Org. Chem. 2011, 76, 9370-9378
DOI: 10.1021/jo201678u
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4-methoxy-<i>trans-beta</i>-nitrostyrene		E Parameter: -14.70
***J. Org. Chem. 2011, 76, 9370-9378
DOI: 10.1021/jo201678u
image of molecule

4-cyano-<i>trans-beta</i>-nitrostyrene		E Parameter: -12.61
***J. Org. Chem. 2011, 76, 9370-9378
DOI: 10.1021/jo201678u
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4-bromo-<i>trans-beta</i>-nitrostyrene		E Parameter: -13.37
***J. Org. Chem. 2011, 76, 9370-9378
DOI: 10.1021/jo201678u
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4-(2,2-bis(phenylsulfonyl)vinyl)-N,N-dimethylaniline		DMSOE Parameter: -16.53
***Chem. Asian J. 2012, 7, 1401-1407
DOI: 10.1002/asia.201101046
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3-methylenetetrahydropyran-2-one		DMSOE Parameter: -19.50
***Chem. Sci. 2021, 12, 4850-4865
DOI: 10.1039/D0SC06628A
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3-methylenedihydrofuranone		DMSOE Parameter: -19.40
***Chem. Sci. 2021, 12, 4850-4865
DOI: 10.1039/D0SC06628A
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3-methylcyclopentenone		DMSOE Parameter: -28.90
*Chem. Sci. 2021, 12, 4850-4865
DOI: 10.1039/D0SC06628A
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3-methylcyclohexenone		DMSOE Parameter: -29.60
*Chem. Sci. 2021, 12, 4850-4865
DOI: 10.1039/D0SC06628A
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2-phenylethene-1-sulfonyl fluoride		DMSOE Parameter: -16.63
***Angew. Chem. Int. Ed. 2016, 55, 12664-12667
DOI: 10.1002/anie.201601875
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2-methylcyclopentenone		DMSOE Parameter: -22.10
***Chem. Sci. 2021, 12, 4850-4865
DOI: 10.1039/D0SC06628A
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2-methylcyclohexenone		DMSOE Parameter: -27.50
*Chem. Sci. 2021, 12, 4850-4865
DOI: 10.1039/D0SC06628A
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2-cinnamoyl-3-methyl-1-(perfluorophenyl)-1H-imidazol-3-ium		DMSOE Parameter: -10.09
***Top. Catal. 2018, 61, 585-590
DOI: 10.1007/s11244-018-0914-5
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2-cinnamoyl-1-mesityl-3-methyl-1H-imidazol-3-ium		DMSOE Parameter: -11.48
***Top. Catal. 2018, 61, 585-590
DOI: 10.1007/s11244-018-0914-5
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2-cinnamoyl-1-(4-methoxyphenyl)-3-methyl-1H-imidazol-3-ium		DMSOE Parameter: -11.79
***Top. Catal. 2018, 61, 585-590
DOI: 10.1007/s11244-018-0914-5
image of molecule

2-cinnamoyl-1-(2,6-dimethoxyphenyl)-3-methyl-1H-imidazol-3-ium		DMSOE Parameter: -12.02
***Top. Catal. 2018, 61, 585-590
DOI: 10.1007/s11244-018-0914-5
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2-cinnamoyl-1,3-dimethyl-1H-imidazol-3-ium		DMSOE Parameter: -11.52
***Angew. Chem. Int. Ed. 2012, 51, 5234-5238
DOI: 10.1002/anie.201109042
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2-benzylidenebenzo[d][1,3]dithiole 1,1,3,3-tetraoxide		DMSOE Parameter: -11.78
***Chem. Asian J. 2012, 7, 1401-1407
DOI: 10.1002/asia.201101046
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2-benzylidene-indan-1,3-dione		0E Parameter: -10.11
***Org. Biomol. Chem. 2007, 5, 3020-3026
DOI: 10.1039/b708025e
image of molecule

2-(p-methoxybenzylidene)-indan-1,3-dione		0E Parameter: -11.32
***Org. Biomol. Chem. 2007, 5, 3020-3026
DOI: 10.1039/b708025e
image of molecule

2-(p-(dimethylamino)benzylidene)-indan-1,3-dione		0E Parameter: -13.56
***Org. Biomol. Chem. 2007, 5, 3020-3026
DOI: 10.1039/b708025e
image of molecule

2-(4-methoxybenzylidene)benzo[d][1,3]dithiole 1,1,3,3-tetraoxide		DMSOE Parameter: -13.02
***Chem. Asian J. 2012, 7, 1401-1407
DOI: 10.1002/asia.201101046
image of molecule

2-(4-methoxybenzylidene)-1,3-dithiane 1,1,3,3-tetraoxide		DMSOE Parameter: -14.55
***Chem. Asian J. 2012, 7, 1401-1407
DOI: 10.1002/asia.201101046
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2,6-diphenyl-4-benzylidenecyclohexa-2,5-dienone		0E Parameter: -11.87
***Eur. J. Org. Chem. 2009, , 3203-3211
DOI: 10.1002/ejoc.200900299
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2,6-dimethyl-4-(4-(dimethylamino)benzylidene)cyclohexa-2,5-dienone		0E Parameter: -16.36
***Eur. J. Org. Chem. 2009, , 3203-3211
DOI: 10.1002/ejoc.200900299
image of molecule

2,6-dimethoxy-4-(4-methoxybenzylidene)cyclohexa-2,5-dienone		0E Parameter: -16.38
***Eur. J. Org. Chem. 2009, , 3203-3211
DOI: 10.1002/ejoc.200900299
image of molecule

2,6-dimethoxy-4-(4-(dimethylamino)benzylidene)cyclohexa-2,5-dienone		0E Parameter: -17.18
***Eur. J. Org. Chem. 2009, , 3203-3211
DOI: 10.1002/ejoc.200900299
image of molecule

2,6-di-tert.butyl-4-(4-nitrobenzylidene)cyclohexa-2,5-dienone		0E Parameter: -14.36
***Eur. J. Org. Chem. 2009, , 3203-3211
DOI: 10.1002/ejoc.200900299
image of molecule

2,6-di-tert.butyl-4-(3-fluorobenzylidene)cyclohexa-2,5-dienone		0E Parameter: -15.03
***Eur. J. Org. Chem. 2009, , 3203-3211
DOI: 10.1002/ejoc.200900299
image of molecule

2,6-di-tert.butyl-4-(3,5-difluorobenzylidene)cyclohexa-2,5-dienone		0E Parameter: -14.50
***Eur. J. Org. Chem. 2009, , 3203-3211
DOI: 10.1002/ejoc.200900299
image of molecule

2,6-di-tert-butyl-4-(2,2,2-trifluoroethylidene)cyclohexa-2,5-dien-1-one		DMSOE Parameter: -11.68
***Eur. J. Org. Chem. 2020, , 3812-3817
DOI: 10.1002/ejoc.202000295
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1-phenylprop-2-en-1-one (in DMSO)		DMSOE Parameter: -15.25
***J. Am. Chem. Soc. 2017, 139, 13318-13329
DOI: 10.1021/jacs.7b05106
image of molecule

1-(tert-butyl)-2-cinnamoyl-3-methyl-1H-imidazol-3-ium		DMSOE Parameter: -11.80
***Top. Catal. 2018, 61, 585-590
DOI: 10.1007/s11244-018-0914-5
image of molecule

1,2-diaza-1,3-diene 1f		MeOHE Parameter: -15.30
*Chem. Eur. J. 2010, 16, 12008-12016
DOI: 10.1002/chem.201000828
image of molecule

1,2-diaza-1,3-diene 1e		MeOHE Parameter: -14.90
*Chem. Eur. J. 2010, 16, 12008-12016
DOI: 10.1002/chem.201000828
image of molecule

1,2-diaza-1,3-diene 1d		DMSOE Parameter: -15.38
***Chem. Eur. J. 2010, 16, 12008-12016
DOI: 10.1002/chem.201000828
image of molecule

1,2-diaza-1,3-diene 1c		DMSOE Parameter: -14.91
***Chem. Eur. J. 2010, 16, 12008-12016
DOI: 10.1002/chem.201000828
image of molecule

1,2-diaza-1,3-diene 1b		DMSOE Parameter: -13.90
***Chem. Eur. J. 2010, 16, 12008-12016
DOI: 10.1002/chem.201000828
image of molecule

1,2-diaza-1,3-diene 1a		DMSOE Parameter: -13.28
***Chem. Eur. J. 2010, 16, 12008-12016
DOI: 10.1002/chem.201000828
image of molecule

(ethene-1,1-diyldisulfonyl)dibenzene		DMSOE Parameter: -7.50
***Chem. Asian J. 2012, 7, 1401-1407
DOI: 10.1002/asia.201101046
image of molecule

(E)-6-benzylidenebenzo[d][1,3]dioxol-5(6H)-one		0E Parameter: -14.47
***Chem. Eur. J. 2024, , e202403785
DOI: 10.1002/chem.202403785
image of molecule

(E)-6-(4-nitrobenzylidene)benzo[d][1,3]dioxol-5(6H)-one		0E Parameter: -13.15
***Chem. Eur. J. 2024, , e202403785
DOI: 10.1002/chem.202403785
image of molecule

(E)-6-(4-methylbenzylidene)benzo[d][1,3]dioxol-5(6H)-one		0E Parameter: -14.85
***Chem. Eur. J. 2024, , e202403785
DOI: 10.1002/chem.202403785
image of molecule

(E)-6-(4-methoxybenzylidene)benzo[d][1,3]dioxol-5(6H)-one		0E Parameter: -15.20
***Chem. Eur. J. 2024, , e202403785
DOI: 10.1002/chem.202403785
image of molecule

(E)-6-(4-chlorobenzylidene)benzo[d][1,3]dioxol-5(6H)-one		0E Parameter: -13.99
***Chem. Eur. J. 2024, , e202403785
DOI: 10.1002/chem.202403785
image of molecule

(E)-6-(4-(trifluoromethyl)benzylidene)benzo[d][1,3]dioxol-5(6H)-one		0E Parameter: -13.54
***Chem. Eur. J. 2024, , e202403785
DOI: 10.1002/chem.202403785
image of molecule

(E)-6-(4-(dimethylamino)benzylidene)benzo[d][1,3]dioxol-5(6H)-one		0E Parameter: -16.07
***Chem. Eur. J. 2024, , e202403785
DOI: 10.1002/chem.202403785
image of molecule

(E)-6-(3-fluorobenzylidene)benzo[d][1,3]dioxol-5(6H)-one		0E Parameter: -14.00
***Chem. Eur. J. 2024, , e202403785
DOI: 10.1002/chem.202403785
image of molecule

(E)-4-phenylbut-3-en-2-one (in DMSO)		DMSOE Parameter: -23.01
***J. Am. Chem. Soc. 2017, 139, 13318-13329
DOI: 10.1021/jacs.7b05106
image of molecule

(E)-4-methyl-1-(4-nitrophenyl)pent-1-en-3-one (in DMSO)		DMSOE Parameter: -19.17
*J. Am. Chem. Soc. 2011, 133, 8240-8251
DOI: 10.1021/ja200820m
image of molecule

(E)-4-(4-nitrophenyl)but-3-en-2-one (in DSMO)		DMSOE Parameter: -19.36
*J. Am. Chem. Soc. 2011, 133, 8240-8251
DOI: 10.1021/ja200820m
image of molecule

(E)-4,4-dimethyl-1-(4-nitrophenyl)pent-1-en-3-one		DMSOE Parameter: -19.15
*J. Am. Chem. Soc. 2011, 133, 8240-8251
DOI: 10.1021/ja200820m
image of molecule

(E)-3-(4-nitro-phenyl)-1-phenyl-prop-2-en-1-one (in DMSO)		DMSOE Parameter: -17.33
***J. Am. Chem. Soc. 2011, 133, 8240-8251
DOI: 10.1021/ja200820m
image of molecule

(E)-3-(4-cyano-phenyl)-1-phenyl-prop-2-en-1-one (in DMSO)		DMSOE Parameter: -17.64
***J. Am. Chem. Soc. 2011, 133, 8240-8251
DOI: 10.1021/ja200820m
image of molecule

(E)-2,6-di-tert-butyl-4-(3-phenylallylidene)cyclohexa-2,5-dien-1-one		DMSOE Parameter: -17.00
***Org. Lett. 2020, 22, 2182-2186
DOI: 10.1021/acs.orglett.0c00338
image of molecule

(E)-2,6-di-tert-butyl-4-(3-(4-nitrophenyl)allylidene)cyclohexa-2,5-dien-1-one		DMSOE Parameter: -16.25
***Org. Lett. 2020, 22, 2182-2186
DOI: 10.1021/acs.orglett.0c00338
image of molecule

(E)-2,6-di-tert-butyl-4-(3-(4-methoxyphenyl)allylidene)cyclohexa-2,5-dien-1-one		DMSOE Parameter: -17.42
***Org. Lett. 2020, 22, 2182-2186
DOI: 10.1021/acs.orglett.0c00338
image of molecule

(E)-1-methyl-4-(styrylsulfonyl)benzene (in DMSO)		DMSOE Parameter: -24.69
**J. Am. Chem. Soc. 2017, 139, 13318-13329
DOI: 10.1021/jacs.7b05106
image of molecule

(E)-1,3-diphenylprop-2-en-1-one (in DMSO)		DMSOE Parameter: -19.39
***J. Am. Chem. Soc. 2017, 139, 13318-13329
DOI: 10.1021/jacs.7b05106
image of molecule

(2-phenylethene-1,1-diyldisulfonyl)dibenzene		DMSOE Parameter: -12.93
***Chem. Asian J. 2012, 7, 1401-1407
DOI: 10.1002/asia.201101046
image of molecule

(2-(4-methoxyphenyl)ethene-1,1-diyldisulfonyl)dibenzene		DMSOE Parameter: -13.88
***Chem. Asian J. 2012, 7, 1401-1407
DOI: 10.1002/asia.201101046
 
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