Electrophiles
Name | Solvent |
Reactivity Parameters |
Classification |
Reference (title or year) |
---|---|---|---|---|
bh 6m | E Param.: -17.30 | Chem. Eur. J. 2010, 16, 1365-1371 10.1002/chem.200902487 | ||
bh6a | E Param.: -18.60 | Chem. Eur. J. 2010, 16, 1365-1371 10.1002/chem.200902487 | ||
bh6j | E Param.: -17.90 | Chem. Eur. J. 2010, 16, 1365-1371 10.1002/chem.200902487 | ||
bis(1,2-dimethylindol-3-yl)methylium ion | E Param.: -10.23 | 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(julidin-9-yl)allylium ion | E Param.: -9.78 | J. Org. Chem. 2011, 76, 9391-9408 10.1021/jo201668w | ||
but-3-en-2-one (in DMSO) | DMSO | E Param.: -16.76 | J. Am. Chem. Soc. 2017, 139, 13318-13329 10.1021/jacs.7b05106 | |
butanal (in DMSO) | DMSO | J. Am. Chem. Soc. 2011, 133, 8240-8251 10.1021/ja200820m | ||
butynone | E Param.: -16.60 | Angew. Chem. Int. Ed. 2019, 58, 17704-17708 10.1002/anie.201909803 | ||
C6H6OMe+-Fe(CO)3 | E Param.: -8.94 | Acc. Chem. Res. 2003, 36, 66-77 10.1021/ar020094c | ||
C6H7+-Fe(CO)3 | E Param.: -7.76 | Acc. Chem. Res. 2003, 36, 66-77 10.1021/ar020094c | ||
C7H7+-Fe(CO)3 | E Param.: -3.49 | Acc. Chem. Res. 2003, 36, 66-77 10.1021/ar020094c | ||
C7H9+-Fe(CO)3 | E Param.: -9.21 | Acc. Chem. Res. 2003, 36, 66-77 10.1021/ar020094c | ||
carbon disulfide | DMSO | E Param.: -17.70 | J. Am. Chem. Soc. 2020, 142, 8383-8402 10.1021/jacs.0c01960 | |
cinnamaldehyde (in DMSO) | DMSO | J. Am. Chem. Soc. 2011, 133, 8240-8251 10.1021/ja200820m | ||
cinnamonitrile (in DMSO) | DMSO | E Param.: -24.60 | J. Am. Chem. Soc. 2017, 139, 13318-13329 10.1021/jacs.7b05106 | |
cumyl cation | E Param.: 5.74 | Macromolecules 2010, 43, 1719-1723 10.1021/ma9024569 | ||
cyclobutanone (in DMSO) | DMSO | E Param.: -17.50 | 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 | |
cycloheptenone | DMSO | E Param.: -22.00 | Chem. Sci. 2021, 12, 4850-4865 10.1039/D0SC06628A | |
cyclohexanone (in DMSO) | DMSO | E Param.: -19.90 | J. Am. Chem. Soc. 2018, 140, 5500-5515 10.1021/jacs.8b01657 | |
cyclohexenone | DMSO | E Param.: -22.10 | Chem. Sci. 2021, 12, 4850-4865 10.1039/D0SC06628A | |
cyclopentanone (in DMSO) | DMSO | E Param.: -21.00 | J. Am. Chem. Soc. 2018, 140, 5500-5515 10.1021/jacs.8b01657 | |
cyclopentenone | DMSO | E Param.: -20.60 | Chem. Sci. 2021, 12, 4850-4865 10.1039/D0SC06628A | |
di-p-anisyl-allylium ion | E Param.: -1.45 | J. Org. Chem. 2011, 76, 9391-9408 10.1021/jo201668w | ||
di-p-tolyl-allylium ion | E Param.: 1.23 | J. Org. Chem. 2011, 76, 9391-9408 10.1021/jo201668w | ||
di-tert-butyl azodicarboxylate | MeCN | E Param.: -12.23 | Chem. Eur. J. 2010, 16, 11670-11677 10.1002/chem.201001598 | |
diarylallylium ion (3,3-F2)2 | E Param.: 6.11 | J. Org. Chem. 2011, 76, 9391-9408 10.1021/jo201668w | ||
diarylallylium ion (3-F)2 | E Param.: 4.15 | J. Org. Chem. 2011, 76, 9391-9408 10.1021/jo201668w | ||
diarylallylium ion (4-Br)2 | E Param.: 2.85 | J. Org. Chem. 2011, 76, 9391-9408 10.1021/jo201668w | ||
diarylallylium ion (4-Cl)2 | E Param.: 2.69 | J. Org. Chem. 2011, 76, 9391-9408 10.1021/jo201668w | ||
diarylallylium ion (4-NMe2)2 | E Param.: -7.50 | J. Org. Chem. 2011, 76, 9391-9408 10.1021/jo201668w | ||
dibenzo[a,d]tropylium ion | dichloromethane | E Param.: -0.63 | Liebigs Ann. 1995, , 2005-2009 10.1002/jlac.1995199[...] | |
dibenzyl azodicarboxylate | MeCN | E Param.: -8.89 | Chem. Eur. J. 2010, 16, 11670-11677 10.1002/chem.201001598 | |
dicarbonyl(cyclopentadienyl)propene-iron(II) | E Param.: -11.20 | Helv. Chim. Acta 2005, 88, 1754-1768 10.1002/hlca.200590137 | ||
diethyl 2-((1-methyl-1,2,3,4-tetrahydroquinolin-6-yl)methylene)malonate | E Param.: -23.40 | Chem. Eur. J. 2008, 14, 9675-9682 10.1002/chem.200801277 | ||
diethyl 2-((julolidine-9-yl)methylene)malonate | E Param.: -23.80 | Chem. Eur. J. 2008, 14, 9675-9682 10.1002/chem.200801277 | ||
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 | ||
methoxy-(4-methoxyphenyl)methylium ion | E Param.: 0.14 | Acc. Chem. Res. 2003, 36, 66-77 10.1021/ar020094c | ||
methoxy-(4-methylphenyl)methylium ion | E Param.: 1.90 | Acc. Chem. Res. 2003, 36, 66-77 10.1021/ar020094c | ||
methoxy-phenylmethylium ion | E Param.: 2.97 | Acc. Chem. Res. 2003, 36, 66-77 10.1021/ar020094c | ||
methyl diazoacetate | E Param.: -18.50 | Chem. Eur. J. 2022, 28, e202201376 10.1002/chem.202201376 | ||
methyl prop-2-enoate (in DMSO) | DMSO | E Param.: -18.84 | J. Am. Chem. Soc. 2017, 139, 13318-13329 10.1021/jacs.7b05106 | |
methyl(phenyl)methyleneammonium ion | E Param.: -5.17 | Acc. Chem. Res. 2003, 36, 66-77 10.1021/ar020094c | ||
mor iminium | E Param.: -8.60 | Angew. Chem. Int. Ed. 2008, 47, 8723-8726 10.1002/anie.200802889 | ||
N,N-dimethylprop-2-enamide (in DMSO) | DMSO | E Param.: -23.54 | J. Am. Chem. Soc. 2017, 139, 13318-13329 10.1021/jacs.7b05106 | |
N-(difluoromethyl)thio)phthalimide | E Param.: -11.86 | Angew. Chem. Int. Ed. 2018, 57, 12690-12695 10.1002/anie.201805859 | ||
N-(phenylsulfonyl)-N-((trifluoromethyl)thio)benzenesulfonamide | E Param.: -6.06 | Angew. Chem. Int. Ed. 2018, 57, 12690-12695 10.1002/anie.201805859 | ||
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 |