Electrophiles
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« Back Forward » Found 375 molecules, displaying page 3 of 8 Results per page
10|50|100|all
| Name | Solvent |
Reactivity Parameters |
Classification |
Reference (title or year) |
|---|---|---|---|---|
dma(t-Bu)2QM![]() ![]() |
E Param.: -17.29 | 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(Ph)2QM![]() ![]() |
E Param.: -13.39 | Angew. Chem. Int. Ed. 2002, 41, 91-95 10.1002/1521-3773(20[...] | ||
diphenyldiazomethane![]() ![]() |
E Param.: -21.40 | Chem. Eur. J. 2022, 28, e202201376 10.1002/chem.202201376 | ||
diphenylcarbodiimide![]() ![]() |
DMSO | E Param.: -20.14 | J. Am. Chem. Soc. 2020, 142, 8383-8402 10.1021/jacs.0c01960 | |
diphenylallylium ion![]() ![]() |
E Param.: 2.70 | J. Org. Chem. 2011, 76, 9391-9408 10.1021/jo201668w | ||
dimethylmethyleneammonium ion![]() ![]() |
E Param.: -6.69 | Acc. Chem. Res. 2003, 36, 66-77 10.1021/ar020094c | ||
dimethyl diazomalonate![]() ![]() |
E Param.: -18.20 | Chem. Eur. J. 2022, 28, e202201376 10.1002/chem.202201376 | ||
diisopropyl azodicarboxylate![]() ![]() |
MeCN | E Param.: -10.71 | Chem. Eur. J. 2010, 16, 11670-11677 10.1002/chem.201001598 | |
dihydro-2H-pyran-2-one![]() ![]() |
DMSO | E Param.: -21.80 | Chem. Sci. 2021, 12, 4850-4865 10.1039/D0SC06628A | |
diethyl maleate![]() ![]() |
DMSO | E Param.: -19.49 | Eur. J. Org. Chem. 2014, , 2956-2963 10.1002/ejoc.201301779 | |
diethyl fumarate![]() ![]() |
DMSO | E Param.: -17.79 | Eur. J. Org. Chem. 2014, , 2956-2963 10.1002/ejoc.201301779 | |
diethyl benzylidene malonate![]() ![]() |
E Param.: -20.55 | 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 4-nitrobenzylidene malonate![]() ![]() |
E Param.: -17.67 | 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-methoxy-benzylidene malonate![]() ![]() |
E Param.: -21.47 | 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-(dimethylamino)benzylidene malonate![]() ![]() |
E Param.: -23.10 | 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 2-((julolidine-9-yl)methylene)malonate![]() ![]() |
E Param.: -23.80 | Chem. Eur. J. 2008, 14, 9675-9682 10.1002/chem.200801277 | ||
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 | ||
dicarbonyl(cyclopentadienyl)propene-iron(II)![]() ![]() |
E Param.: -11.20 | Helv. Chim. Acta 2005, 88, 1754-1768 10.1002/hlca.200590137 | ||
dibenzyl azodicarboxylate![]() ![]() |
MeCN | E Param.: -8.89 | Chem. Eur. J. 2010, 16, 11670-11677 10.1002/chem.201001598 | |
dibenzo[a,d]tropylium ion![]() ![]() |
dichloromethane | E Param.: -0.63 | Liebigs Ann. 1995, , 2005-2009 10.1002/jlac.1995199[...] | |
diarylallylium ion (4-NMe2)2![]() ![]() |
E Param.: -7.50 | 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-Br)2![]() ![]() |
E Param.: 2.85 | 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 (3,3-F2)2![]() ![]() |
E Param.: 6.11 | 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 | |
di-p-tolyl-allylium ion![]() ![]() |
E Param.: 1.23 | J. Org. Chem. 2011, 76, 9391-9408 10.1021/jo201668w | ||
di-p-anisyl-allylium ion![]() ![]() |
E Param.: -1.45 | J. Org. Chem. 2011, 76, 9391-9408 10.1021/jo201668w | ||
cyclopentenone![]() ![]() |
DMSO | E Param.: -20.60 | 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 | |
cyclohexenone![]() ![]() |
DMSO | E Param.: -22.10 | 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 | |
cycloheptenone![]() ![]() |
DMSO | E Param.: -22.00 | Chem. Sci. 2021, 12, 4850-4865 10.1039/D0SC06628A | |
cycloheptanone (in DMSO)![]() ![]() |
DMSO | E Param.: -22.10 | J. Am. Chem. Soc. 2018, 140, 5500-5515 10.1021/jacs.8b01657 | |
cyclobutanone (in DMSO)![]() ![]() |
DMSO | E Param.: -17.50 | J. Am. Chem. Soc. 2018, 140, 5500-5515 10.1021/jacs.8b01657 | |
cumyl cation![]() ![]() |
E Param.: 5.74 | Macromolecules 2010, 43, 1719-1723 10.1021/ma9024569 | ||
cinnamonitrile (in DMSO)![]() ![]() |
DMSO | E Param.: -24.60 | J. Am. Chem. Soc. 2017, 139, 13318-13329 10.1021/jacs.7b05106 | |
cinnamaldehyde (in DMSO)![]() ![]() |
DMSO | J. Am. Chem. Soc. 2011, 133, 8240-8251 10.1021/ja200820m | ||
carbon disulfide![]() ![]() |
DMSO | E Param.: -17.70 | J. Am. Chem. Soc. 2020, 142, 8383-8402 10.1021/jacs.0c01960 | |
C7H9+-Fe(CO)3![]() ![]() |
E Param.: -9.21 | 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 | ||
C6H7+-Fe(CO)3![]() ![]() |
E Param.: -7.76 | Acc. Chem. Res. 2003, 36, 66-77 10.1021/ar020094c | ||
C6H6OMe+-Fe(CO)3![]() ![]() |
E Param.: -8.94 | Acc. Chem. Res. 2003, 36, 66-77 10.1021/ar020094c | ||
butynone![]() ![]() |
E Param.: -16.60 | Angew. Chem. Int. Ed. 2019, 58, 17704-17708 10.1002/anie.201909803 | ||
butanal (in DMSO)![]() ![]() |
DMSO | J. Am. Chem. Soc. 2011, 133, 8240-8251 10.1021/ja200820m |



















































