Electrophiles
| Name | Solvent |
Reactivity Parameters |
Classification |
Reference (title or year) |
|---|---|---|---|---|
2,5-dichloroquinone (C-H) ![]() |
E Param.: -12.28 |
J. Am. Chem. Soc. 2014, 136, 11499-11512 10.1021/ja505613b |
||
2,5-dichloroquinone (C-Cl) ![]() |
E Param.: -16.11 |
J. Am. Chem. Soc. 2014, 136, 11499-11512 10.1021/ja505613b |
||
p-chloranil (C=O) ![]() |
E Param.: -12.13 |
J. Am. Chem. Soc. 2014, 136, 11499-11512 10.1021/ja505613b |
||
p-chloranil (C-Cl) ![]() |
E Param.: -13.84 |
J. Am. Chem. Soc. 2014, 136, 11499-11512 10.1021/ja505613b |
||
p-fluoranil (C=O) ![]() |
E Param.: -9.37 |
J. Am. Chem. Soc. 2014, 136, 11499-11512 10.1021/ja505613b |
||
p-fluoranil (C-F) ![]() |
E Param.: -11.12 |
J. Am. Chem. Soc. 2014, 136, 11499-11512 10.1021/ja505613b |
||
o-chloranil (C=O) ![]() |
E Param.: -8.77 |
J. Am. Chem. Soc. 2014, 136, 11499-11512 10.1021/ja505613b |
||
o-chloranil (C-Cl) ![]() |
E Param.: -12.02 |
J. Am. Chem. Soc. 2014, 136, 11499-11512 10.1021/ja505613b |
||
3-benzylidene-1-methyl-3H-indol-1-ium ion ![]() |
E Param.: -1.80 |
J. Org. Chem. 2015, 80, 8643-8656 10.1021/acs.joc.5b01298 |
||
1-methyl-3-(4-methylbenzylidene)-3H-indol-1-ium ion ![]() |
E Param.: -2.19 |
J. Org. Chem. 2015, 80, 8643-8656 10.1021/acs.joc.5b01298 |
||
3-(4-methoxybenzylidene)-1-methyl-3H-indol-1-ium iom ![]() |
E Param.: -3.02 |
J. Org. Chem. 2015, 80, 8643-8656 10.1021/acs.joc.5b01298 |
||
3-(4-(dimethylamino)benzylidene)-1-methyl-3H-indol-1-ium ion ![]() |
E Param.: -6.26 |
J. Org. Chem. 2015, 80, 8643-8656 10.1021/acs.joc.5b01298 |
||
1-methyl-3-((julolidin-9-yl)methylene)-3H-indol-1-ium ion ![]() |
E Param.: -7.79 |
J. Org. Chem. 2015, 80, 8643-8656 10.1021/acs.joc.5b01298 |
||
(E)-2-methyl-3-(4-methylbenzylidene)-3H-indol-1-ium ion ![]() |
E Param.: -5.15 |
J. Org. Chem. 2015, 80, 8643-8656 10.1021/acs.joc.5b01298 |
||
(E)-1,2-dimethyl-3-(4-methylbenzylidene)-3H-indol-1-ium ion ![]() |
E Param.: -5.05 |
J. Org. Chem. 2015, 80, 8643-8656 10.1021/acs.joc.5b01298 |
||
(E)-3-benzylidene-1,2-dimethyl-3H-indol-1-ium ion ![]() |
E Param.: -4.96 |
J. Org. Chem. 2015, 80, 8643-8656 10.1021/acs.joc.5b01298 |
||
bis(1-methylindol-3-yl)methylium ion ![]() |
E Param.: -5.99 |
J. Org. Chem. 2015, 80, 8643-8656 10.1021/acs.joc.5b01298 |
||
bis(5-methoxy-1-methylindol-3-yl)methylium ion ![]() |
E Param.: -6.90 |
J. Org. Chem. 2015, 80, 8643-8656 10.1021/acs.joc.5b01298 |
||
bis(1,2-dimethylindol-3-yl)methylium ion ![]() |
E Param.: -10.23 |
J. Org. Chem. 2015, 80, 8643-8656 10.1021/acs.joc.5b01298 |
||
dibenzo[a,d]tropylium ion ![]() |
dichloromethane | E Param.: -0.63 |
Liebigs Ann. 1995, , 2005-2009 10.1002/jlac.1995199[...] |
|
ethenesulfonyl fluoride (ESF) ![]() |
DMSO | E Param.: -12.09 |
Angew. Chem. Int. Ed. 2016, 55, 12664-12667 10.1002/anie.201601875 |
|
2-phenylethene-1-sulfonyl fluoride ![]() |
DMSO | E Param.: -16.63 |
Angew. Chem. Int. Ed. 2016, 55, 12664-12667 10.1002/anie.201601875 |
|
(E)-2-(tert-butyl)-3-(4-methylbenzylidene)-3H-indol-1-ium ![]() |
dichloromethane | E Param.: -5.06 |
Eur. J. Org. Chem. 2016, , 4050-4058 10.1002/ejoc.201600572 |
|
9-phenyl-9H-fluoren-9-ylium ![]() |
dichloromethane | E Param.: 2.41 |
Chem. Eur. J. 2017, 23, 623-630 10.1002/chem.201603963 |
|
9-(4-methoxyphenyl)-9H-fluoren-9-ylium ![]() |
dichloromethane | E Param.: 0.85 |
Chem. Eur. J. 2017, 23, 623-630 10.1002/chem.201603963 |
|
9-(4-(dimethylamino)phenyl)-9H-fluoren-9-ylium ![]() |
dichloromethane | E Param.: -4.51 |
Chem. Eur. J. 2017, 23, 623-630 10.1002/chem.201603963 |
|
(E)-4-phenylbut-3-en-2-one (in DMSO) ![]() |
DMSO | E Param.: -23.01 |
J. Am. Chem. Soc. 2017, 139, 13318-13329 10.1021/jacs.7b05106 |
|
cinnamonitrile (in DMSO) ![]() |
DMSO | E Param.: -24.60 |
J. Am. Chem. Soc. 2017, 139, 13318-13329 10.1021/jacs.7b05106 |
|
methyl prop-2-enoate (in DMSO) ![]() |
DMSO | E Param.: -18.84 |
J. Am. Chem. Soc. 2017, 139, 13318-13329 10.1021/jacs.7b05106 |
|
ethyl prop-2-enoate (in DMSO) ![]() |
DMSO | E Param.: -19.07 |
J. Am. Chem. Soc. 2017, 139, 13318-13329 10.1021/jacs.7b05106 |
|
tert-butyl prop-2-enoate (in DMSO) ![]() |
DMSO | E Param.: -20.22 |
J. Am. Chem. Soc. 2017, 139, 13318-13329 10.1021/jacs.7b05106 |
|
N,N-dimethylprop-2-enamide (in DMSO) ![]() |
DMSO | E Param.: -23.54 |
J. Am. Chem. Soc. 2017, 139, 13318-13329 10.1021/jacs.7b05106 |
|
ethenylsulfonylbenzene (in DMSO) ![]() |
DMSO | E Param.: -18.36 |
J. Am. Chem. Soc. 2017, 139, 13318-13329 10.1021/jacs.7b05106 |
|
acrylonitrile (in DMSO) ![]() |
DMSO | E Param.: -19.05 |
J. Am. Chem. Soc. 2017, 139, 13318-13329 10.1021/jacs.7b05106 |
|
but-3-en-2-one (in DMSO) ![]() |
DMSO | E Param.: -16.76 |
J. Am. Chem. Soc. 2017, 139, 13318-13329 10.1021/jacs.7b05106 |
|
1-phenylprop-2-en-1-one (in DMSO) ![]() |
DMSO | E Param.: -15.25 |
J. Am. Chem. Soc. 2017, 139, 13318-13329 10.1021/jacs.7b05106 |
|
ethyl 2-methylprop-2-enoate (in DMSO) ![]() |
DMSO | E Param.: -22.77 |
J. Am. Chem. Soc. 2017, 139, 13318-13329 10.1021/jacs.7b05106 |
|
ethyl (E)-but-2-enoate (in DMSO) ![]() |
DMSO | E Param.: -23.59 |
J. Am. Chem. Soc. 2017, 139, 13318-13329 10.1021/jacs.7b05106 |
|
ethyl cinnamate (in DMSO) ![]() |
DMSO | E Param.: -24.52 |
J. Am. Chem. Soc. 2017, 139, 13318-13329 10.1021/jacs.7b05106 |
|
(E)-1-methyl-4-(styrylsulfonyl)benzene (in DMSO) ![]() |
DMSO | E Param.: -24.69 |
J. Am. Chem. Soc. 2017, 139, 13318-13329 10.1021/jacs.7b05106 |
|
2-cinnamoyl-3-methyl-1-(perfluorophenyl)-1H-imidazol-3-ium ![]() |
DMSO | E Param.: -10.09 |
Top. Catal. 2018, 61, 585-590 10.1007/s11244-018-0[...] |
|
1-(tert-butyl)-2-cinnamoyl-3-methyl-1H-imidazol-3-ium ![]() |
DMSO | E Param.: -11.80 |
Top. Catal. 2018, 61, 585-590 10.1007/s11244-018-0[...] |
|
2-cinnamoyl-1-mesityl-3-methyl-1H-imidazol-3-ium ![]() |
DMSO | E Param.: -11.48 |
Top. Catal. 2018, 61, 585-590 10.1007/s11244-018-0[...] |
|
2-cinnamoyl-1-(4-methoxyphenyl)-3-methyl-1H-imidazol-3-ium ![]() |
DMSO | E Param.: -11.79 |
Top. Catal. 2018, 61, 585-590 10.1007/s11244-018-0[...] |
|
2-cinnamoyl-1-(2,6-dimethoxyphenyl)-3-methyl-1H-imidazol-3-ium ![]() |
DMSO | E Param.: -12.02 |
Top. Catal. 2018, 61, 585-590 10.1007/s11244-018-0[...] |
|
cyclobutanone (in DMSO) ![]() |
DMSO | E Param.: -17.50 |
J. Am. Chem. Soc. 2018, 140, 5500-5515 10.1021/jacs.8b01657 |
|
cyclopentanone (in DMSO) ![]() |
DMSO | E Param.: -21.00 |
J. Am. Chem. Soc. 2018, 140, 5500-5515 10.1021/jacs.8b01657 |
|
cyclohexanone (in DMSO) ![]() |
DMSO | E Param.: -19.90 |
J. Am. Chem. Soc. 2018, 140, 5500-5515 10.1021/jacs.8b01657 |
|
cycloheptanone (in DMSO) ![]() |
DMSO | E Param.: -22.10 |
J. Am. Chem. Soc. 2018, 140, 5500-5515 10.1021/jacs.8b01657 |
|
1-methylpiperidin-4-one (in DMSO) ![]() |
DMSO | E Param.: -18.40 |
J. Am. Chem. Soc. 2018, 140, 5500-5515 10.1021/jacs.8b01657 |

