Electrophiles
Name | Solvent |
Reactivity Parameters |
Classification |
Reference (title or year) |
---|---|---|---|---|
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 | ||
N-(phenylsulfonyl)-N-((trifluoromethyl)thio)benzenesulfonamide | E Param.: -6.06 | Angew. Chem. Int. Ed. 2018, 57, 12690-12695 10.1002/anie.201805859 | ||
N-fluoro-2,4,6-trimethylpyridinium tetrafluoroborate | E Param.: -10.46 | J. Am. Chem. Soc. 2018, 140, 11474-11486 10.1021/jacs.8b07147 | ||
N-fluoro-2,6-dichloropyridinium tetrafluoroborate | E Param.: -5.29 | J. Am. Chem. Soc. 2018, 140, 11474-11486 10.1021/jacs.8b07147 | ||
Selectfluor | E Param.: -5.20 | J. Am. Chem. Soc. 2018, 140, 11474-11486 10.1021/jacs.8b07147 | ||
N-fluoropyridinium tetrafluoroborate | E Param.: -9.89 | J. Am. Chem. Soc. 2018, 140, 11474-11486 10.1021/jacs.8b07147 | ||
N-(trifluoromethyl)thio)phthalimide | E Param.: -11.92 | Angew. Chem. Int. Ed. 2018, 57, 12690-12695 10.1002/anie.201805859 | ||
N-(trifluoromethyl)thio)saccharin | E Param.: -6.48 | Angew. Chem. Int. Ed. 2018, 57, 12690-12695 10.1002/anie.201805859 | ||
N-(trifluoromethyl)thio)succinimide | E Param.: -12.56 | Angew. Chem. Int. Ed. 2018, 57, 12690-12695 10.1002/anie.201805859 | ||
N-(difluoromethyl)thio)phthalimide | E Param.: -11.86 | Angew. Chem. Int. Ed. 2018, 57, 12690-12695 10.1002/anie.201805859 | ||
N-methyl-N-((trifluoromethyl)thio)-p-toluenesulfonamide | E Param.: -13.44 | Angew. Chem. Int. Ed. 2018, 57, 12690-12695 10.1002/anie.201805859 | ||
N-methyl-N-((trifluoromethyl)thio)-aniline | E Param.: -23.32 | Angew. Chem. Int. Ed. 2018, 57, 12690-12695 10.1002/anie.201805859 | ||
((2-phenylpropan-2-yl)oxy)(trifluoromethyl)sulfane | E Param.: -13.77 | Angew. Chem. Int. Ed. 2018, 57, 12690-12695 10.1002/anie.201805859 | ||
((2-(2-iodophenyl)propan-2-yl)oxy)(trifluoromethyl)sulfane | E Param.: -14.52 | Angew. Chem. Int. Ed. 2018, 57, 12690-12695 10.1002/anie.201805859 | ||
ethyl 3-nitro-1H-indole-1-carboxylate | E Param.: -14.10 | Chem. Commun. 2021, 57, 10071-10074 10.1039/d1cc04074j | ||
3-nitro-1-tosyl-1H-indole | E Param.: -14.87 | Chem. Commun. 2021, 57, 10071-10074 10.1039/d1cc04074j | ||
4-bromo-3-nitro-1-tosyl-1H-indole | E Param.: -14.60 | Chem. Commun. 2021, 57, 10071-10074 10.1039/d1cc04074j | ||
3,6-dinitro-1-tosyl-1H-indole | E Param.: -12.90 | Chem. Commun. 2021, 57, 10071-10074 10.1039/d1cc04074j | ||
4-phenylbut-3-yn-2-one | E Param.: -16.90 | Angew. Chem. Int. Ed. 2019, 58, 17704-17708 10.1002/anie.201909803 | ||
hex-3-yn-2-one | E Param.: -17.90 | Angew. Chem. Int. Ed. 2019, 58, 17704-17708 10.1002/anie.201909803 | ||
methyl diazoacetate | E Param.: -18.50 | Chem. Eur. J. 2022, 28, e202201376 10.1002/chem.202201376 | ||
dimethyl diazomalonate | E Param.: -18.20 | Chem. Eur. J. 2022, 28, e202201376 10.1002/chem.202201376 | ||
(p-nitrophenyl)diazomethane | E Param.: -18.30 | Chem. Eur. J. 2022, 28, e202201376 10.1002/chem.202201376 | ||
diphenyldiazomethane | E Param.: -21.40 | Chem. Eur. J. 2022, 28, e202201376 10.1002/chem.202201376 | ||
butynone | E Param.: -16.60 | Angew. Chem. Int. Ed. 2019, 58, 17704-17708 10.1002/anie.201909803 | ||
Umemoto I (triflate) | E Param.: -13.08 | Eur. J. Org. Chem. 2024, 27, e202400085 10.1002/ejoc.202400085 | ||
Umemoto I (tetrafluoroborate) | E Param.: -13.39 | Eur. J. Org. Chem. 2024, 27, e202400085 10.1002/ejoc.202400085 | ||
Umemoto II (triflate) | E Param.: -12.80 | Eur. J. Org. Chem. 2024, 27, e202400085 10.1002/ejoc.202400085 | ||
ani(t-Bu)2QM | E Param.: -16.11 | Angew. Chem. Int. Ed. 2002, 41, 91-95 10.1002/1521-3773(20[...] | ||
dma(t-Bu)2QM | E Param.: -17.29 | Angew. Chem. Int. Ed. 2002, 41, 91-95 10.1002/1521-3773(20[...] | ||
cumyl cation | E Param.: 5.74 | Macromolecules 2010, 43, 1719-1723 10.1021/ma9024569 | ||
(4-CF3)2-tritylium ion | E Param.: 2.28 | J. Am. Chem. Soc. 2003, 125, 286-295 10.1021/ja021010y | ||
(3-Cl)3-tritylium ion | E Param.: 1.99 | J. Am. Chem. Soc. 2003, 125, 286-295 10.1021/ja021010y | ||
(4-CF3)-tritylium ion | E Param.: 1.33 | J. Am. Chem. Soc. 2003, 125, 286-295 10.1021/ja021010y | ||
(3-Cl)-tritylium ion | E Param.: 1.06 | J. Am. Chem. Soc. 2003, 125, 286-295 10.1021/ja021010y | ||
(3-CF3)-tritylium ion | E Param.: 1.18 | J. Am. Chem. Soc. 2003, 125, 286-295 10.1021/ja021010y | ||
(4-Me)-tritylium ion | E Param.: -0.13 | J. Am. Chem. Soc. 2003, 125, 286-295 10.1021/ja021010y | ||
(4-Me)2-tritylium ion | E Param.: -0.70 | J. Am. Chem. Soc. 2003, 125, 286-295 10.1021/ja021010y | ||
(4-Me)3-tritylium ion | E Param.: -1.21 | J. Am. Chem. Soc. 2003, 125, 286-295 10.1021/ja021010y | ||
(4-MeO,3-OMe)-tritylium ion | E Param.: -1.62 | J. Am. Chem. Soc. 2003, 125, 286-295 10.1021/ja021010y |