Electrophiles
Name | Solvent |
Reactivity Parameters |
Classification |
Reference (title or year) |
---|---|---|---|---|
diethyl 3-chloro-benzylidene malonate![]() ![]() |
E Param.: -18.98 | ![]() ![]() ![]() | Chem. Eur. J. 2008, 14, 9675-9682 10.1002/chem.200801277 | |
diethyl 4-(dimethylamino)benzylidene malonate![]() ![]() |
E Param.: -23.10 | ![]() ![]() ![]() | Chem. Eur. J. 2008, 14, 9675-9682 10.1002/chem.200801277 | |
diethyl 4-cyano-benzylidene malonate![]() ![]() |
E Param.: -18.06 | ![]() ![]() ![]() | Chem. Eur. J. 2008, 14, 9675-9682 10.1002/chem.200801277 | |
diethyl 4-methoxy-benzylidene malonate![]() ![]() |
E Param.: -21.47 | ![]() ![]() ![]() | Chem. Eur. J. 2008, 14, 9675-9682 10.1002/chem.200801277 | |
diethyl 4-methyl-benzylidene malonate![]() ![]() |
E Param.: -21.11 | ![]() ![]() ![]() | Chem. Eur. J. 2008, 14, 9675-9682 10.1002/chem.200801277 | |
diethyl 4-nitrobenzylidene malonate![]() ![]() |
E Param.: -17.67 | ![]() ![]() ![]() | Chem. Eur. J. 2008, 14, 9675-9682 10.1002/chem.200801277 | |
diethyl azodicarboxylate![]() ![]() |
MeCN | E Param.: -10.15 | ![]() ![]() ![]() | Chem. Eur. J. 2010, 16, 11670-11677 10.1002/chem.201001598 |
diethyl benzylidene malonate![]() ![]() |
E Param.: -20.55 | ![]() ![]() ![]() | Chem. Eur. J. 2008, 14, 9675-9682 10.1002/chem.200801277 | |
diethyl fumarate![]() ![]() |
DMSO | E Param.: -17.79 | ![]() ![]() ![]() | Eur. J. Org. Chem. 2014, , 2956-2963 10.1002/ejoc.201301779 |
diethyl maleate![]() ![]() |
DMSO | E Param.: -19.49 | ![]() ![]() ![]() | Eur. J. Org. Chem. 2014, , 2956-2963 10.1002/ejoc.201301779 |
dihydro-2H-pyran-2-one![]() ![]() |
DMSO | E Param.: -21.80 | ![]() ![]() | Chem. Sci. 2021, 12, 4850-4865 10.1039/D0SC06628A |
diisopropyl azodicarboxylate![]() ![]() |
MeCN | E Param.: -10.71 | ![]() ![]() ![]() | Chem. Eur. J. 2010, 16, 11670-11677 10.1002/chem.201001598 |
dimethyl diazomalonate![]() ![]() |
E Param.: -18.20 | ![]() ![]() ![]() | Chem. Eur. J. 2022, 28, e202201376 10.1002/chem.202201376 | |
dimethylmethyleneammonium ion![]() ![]() |
E Param.: -6.69 | ![]() | Acc. Chem. Res. 2003, 36, 66-77 10.1021/ar020094c | |
diphenylallylium ion![]() ![]() |
E Param.: 2.70 | ![]() ![]() ![]() | J. Org. Chem. 2011, 76, 9391-9408 10.1021/jo201668w | |
diphenylcarbodiimide![]() ![]() |
DMSO | E Param.: -20.14 | ![]() ![]() ![]() | J. Am. Chem. Soc. 2020, 142, 8383-8402 10.1021/jacs.0c01960 |
diphenyldiazomethane![]() ![]() |
E Param.: -21.40 | ![]() | Chem. Eur. J. 2022, 28, e202201376 10.1002/chem.202201376 | |
dma(Ph)2QM![]() ![]() |
E Param.: -13.39 | ![]() ![]() ![]() ![]() | Angew. Chem. Int. Ed. 2002, 41, 91-95 10.1002/1521-3773(20[...] | |
dma(S)BBS![]() ![]() |
E Param.: -10.73 | ![]() ![]() ![]() | J. Org. Chem. 2007, 72, 9170-9180 10.1021/jo071273g | |
dma(t-Bu)2QM![]() ![]() |
E Param.: -17.29 | ![]() ![]() ![]() ![]() | Angew. Chem. Int. Ed. 2002, 41, 91-95 10.1002/1521-3773(20[...] | |
dmaBBS![]() ![]() |
E Param.: -12.76 | ![]() ![]() ![]() | J. Org. Chem. 2007, 72, 9170-9180 10.1021/jo071273g | |
E)-2,6-di-tert-butyl-4-(3-(4-chlorophenyl)allylidene)cyclohexa-2,5-dien-1-one![]() ![]() |
DMSO | E Param.: -16.84 | ![]() ![]() ![]() | Org. Lett. 2020, 22, 2182-2186 10.1021/acs.orglett.[...] |
ethenesulfonyl fluoride (ESF)![]() ![]() |
DMSO | E Param.: -12.09 | ![]() ![]() ![]() | Angew. Chem. Int. Ed. 2016, 55, 12664-12667 10.1002/anie.201601875 |
ethenylsulfonylbenzene (in DMSO)![]() ![]() |
DMSO | E Param.: -18.36 | ![]() ![]() ![]() | 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 2-methylprop-2-enoate (in DMSO)![]() ![]() |
DMSO | E Param.: -22.77 | ![]() ![]() | J. Am. Chem. Soc. 2017, 139, 13318-13329 10.1021/jacs.7b05106 |
ethyl 3-nitro-1H-indole-1-carboxylate![]() ![]() |
E Param.: -14.10 | ![]() ![]() | Chem. Commun. 2021, 57, 10071-10074 10.1039/d1cc04074j | |
ethyl cinnamate (in DMSO)![]() ![]() |
DMSO | E Param.: -24.52 | ![]() ![]() | 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 |
fc(ani)CH+![]() ![]() |
E Param.: -2.90 | ![]() ![]() ![]() | Acc. Chem. Res. 2003, 36, 66-77 10.1021/ar020094c | |
fc(Me)CH+![]() ![]() |
E Param.: -2.57 | ![]() | Acc. Chem. Res. 2003, 36, 66-77 10.1021/ar020094c | |
fc(Ph)CH+![]() ![]() |
E Param.: -2.64 | ![]() ![]() ![]() ![]() ![]() | J. Am. Chem. Soc. 2001, 123, 9500-9512 10.1021/ja010890y | |
fc2CH+![]() ![]() |
E Param.: -8.54 | ![]() ![]() ![]() | Acc. Chem. Res. 2003, 36, 66-77 10.1021/ar020094c | |
flavylium ion![]() ![]() |
E Param.: -3.45 | ![]() ![]() ![]() | Acc. Chem. Res. 2003, 36, 66-77 10.1021/ar020094c | |
fumaronitrile![]() ![]() |
DMSO | E Param.: -15.71 | ![]() ![]() ![]() | Eur. J. Org. Chem. 2014, , 2956-2963 10.1002/ejoc.201301779 |
furan-2(5H)-one![]() ![]() |
DMSO | E Param.: -20.70 | ![]() ![]() ![]() | Chem. Sci. 2021, 12, 4850-4865 10.1039/D0SC06628A |
hex-3-yn-2-one![]() ![]() |
E Param.: -17.90 | ![]() | Angew. Chem. Int. Ed. 2019, 58, 17704-17708 10.1002/anie.201909803 | |
hexanal (in DMSO)![]() ![]() |
DMSO | ![]() | J. Am. Chem. Soc. 2011, 133, 8240-8251 10.1021/ja200820m | |
indolecarboxylate derived iminium ion![]() ![]() |
dichloromethane | E Param.: -9.50 | ![]() ![]() | Angew. Chem. Int. Ed. 2009, 48, 5034-5037 10.1002/anie.200900933 |
Jorgensen/Hayashi-iminium ion![]() ![]() |
E Param.: -8.20 | ![]() ![]() ![]() | Angew. Chem. Int. Ed. 2008, 47, 8723-8726 10.1002/anie.200802889 | |
jul Meldrum's acid![]() ![]() |
E Param.: -13.97 | ![]() ![]() ![]() | J. Org. Chem. 2008, 73, 2738-2745 10.1021/jo702590s | |
jul(S)BBS![]() ![]() |
E Param.: -11.89 | ![]() ![]() ![]() | J. Org. Chem. 2007, 72, 9170-9180 10.1021/jo071273g | |
jul(t-Bu)2QM![]() ![]() |
E Param.: -17.90 | ![]() ![]() ![]() ![]() | Angew. Chem. Int. Ed. 2002, 41, 91-95 10.1002/1521-3773(20[...] | |
jul-indan-1,3-dione![]() ![]() |
E Param.: -14.68 | ![]() ![]() ![]() | Org. Biomol. Chem. 2007, 5, 3020-3026 10.1039/b708025e | |
julBBS![]() ![]() |
E Param.: -13.84 | ![]() ![]() ![]() | J. Org. Chem. 2007, 72, 9170-9180 10.1021/jo071273g | |
MacMillan-iminium ion (1st generation)![]() ![]() |
MeCN | E Param.: -7.37 | ![]() ![]() ![]() | Angew. Chem. Int. Ed. 2011, 50, 9953-9956 10.1002/anie.201103683 |
MacMillan-iminium ion (2nd generation)![]() ![]() |
MeCN | E Param.: -5.52 | ![]() ![]() ![]() | Angew. Chem. Int. Ed. 2011, 50, 9953-9956 10.1002/anie.201103683 |
MacMillan-iminium ion (spiro)![]() ![]() |
MeCN | E Param.: -7.67 | ![]() ![]() ![]() | Angew. Chem. Int. Ed. 2011, 50, 9953-9956 10.1002/anie.201103683 |
maleic anhydride![]() ![]() |
DMSO | E Param.: -11.31 | ![]() ![]() ![]() | Eur. J. Org. Chem. 2014, , 2956-2963 10.1002/ejoc.201301779 |
Me2N+=CH-CH-Ph![]() ![]() |
E Param.: -9.20 | ![]() ![]() ![]() | Angew. Chem. Int. Ed. 2008, 47, 8723-8726 10.1002/anie.200802889 |