Electrophiles
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« Back Forward » Found 367 molecules, displaying page 6 of 8 Results per page
10|50|100|all
| 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 |