C-Nucleophiles
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« Back Forward » Found 572 molecules, displaying page 22 of 29 Results per page
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Name | Solvent |
Reactivity Parameters |
Classification |
Reference (title or year) |
---|---|---|---|---|
anion of 2-phenyl-2-(phenylsulfonyl)acetonitrile (in DMSO)![]() ![]() |
DMSO | N Param.: 15.97 sN Param.: 0.72 | ![]() ![]() ![]() | Eur. J. Org. Chem. 2017, , 1196-1202 10.1002/ejoc.201601513 |
anion of ethyl acetylacetate (in water)![]() ![]() |
water | N Param.: 15.99 sN Param.: 0.62 | ![]() ![]() ![]() | J. Am. Chem. Soc. 2003, 125, 12980-12986 10.1021/ja036838e |
anion of 1-phenylbutane-1,3-dione (in DMSO)![]() ![]() |
DMSO | N Param.: 16.03 sN Param.: 0.86 | ![]() ![]() ![]() | Chem. Eur. J. 2015, 21, 875-884 10.1002/chem.201404500 |
2H-benzo[d][1,3]dithiol-2-ide 1,1,3,3-tetraoxide (in DMSO)![]() ![]() |
DMSO | N Param.: 16.06 sN Param.: 0.69 | ![]() ![]() ![]() | Angew. Chem. Int. Ed. 2016, 55, 12845-12848 10.1002/anie.201605616 |
anion of diethyl malonate (in water)![]() ![]() |
water | N Param.: 16.15 sN Param.: 0.66 | ![]() ![]() ![]() | J. Am. Chem. Soc. 2003, 125, 12980-12986 10.1021/ja036838e |
anion of 4-(trifluoromethyl)benzyl trifluoromethyl sulfone (in MeCN)![]() ![]() |
MeCN | N Param.: 16.15 sN Param.: 0.99 | ![]() ![]() ![]() | J. Am. Chem. Soc. 2020, 142, 8383-8402 10.1021/jacs.0c01960 |
Me2S=CH-CN (in DMSO)![]() ![]() |
DMSO | N Param.: 16.23 sN Param.: 0.60 | ![]() ![]() ![]() | Chem. Eur. J. 2010, 16, 8610-8614 10.1002/chem.201001455 |
1-ethoxy-3-(4-nitrophenyl)-1,3-dioxopropan-2-ide (in DMSO)![]() ![]() |
DMSO | N Param.: 16.26 sN Param.: 0.83 | ![]() ![]() ![]() | J. Am. Chem. Soc. 2018, 140, 11474-11486 10.1021/jacs.8b07147 |
anion of dimedone (in DMSO)![]() ![]() |
DMSO | N Param.: 16.27 sN Param.: 0.77 | ![]() ![]() ![]() | Angew. Chem. Int. Ed. 2002, 41, 91-95 10.1002/1521-3773(20[...] |
cyanide (in MeCN)![]() ![]() |
MeCN | N Param.: 16.27 sN Param.: 0.70 | ![]() ![]() ![]() | Angew. Chem. Int. Ed. 2005, 44, 142-145 10.1002/anie.200461640 |
anion of 4-cyanobenzyl trifluoromethyl sulfone (in DMSO)![]() ![]() |
DMSO | N Param.: 16.28 sN Param.: 0.75 | ![]() ![]() ![]() | J. Am. Chem. Soc. 2007, 129, 9753-9761 10.1021/ja072135b |
anion of (4-nitrophenyl)nitromethane (in DMSO)![]() ![]() |
DMSO | N Param.: 16.29 sN Param.: 0.75 | ![]() ![]() ![]() | J. Org. Chem. 2004, 69, 7565-7576 10.1021/jo048773j |
1-(N-pyrrolidino)cyclohexene (in MeCN)![]() ![]() |
MeCN | N Param.: 16.42 sN Param.: 0.70 | ![]() ![]() ![]() | Angew. Chem. Int. Ed. 2010, 49, 9526-9529 10.1002/anie.201004344 |
3-(tert-butyl)-1-methyl-1H-imidazol-3-ium-2-ide (in THF)![]() ![]() |
THF | N Param.: 16.54 sN Param.: 0.47 | ![]() ![]() ![]() | Org. Lett. 2016, 18, 3566-3569 10.1021/acs.orglett.[...] |
anion of 3-oxo-3-phenylpropanenitrile (in DMSO)![]() ![]() |
DMSO | N Param.: 16.55 sN Param.: 0.78 | ![]() ![]() ![]() | Chem. Eur. J. 2015, 21, 875-884 10.1002/chem.201404500 |
MeO-Breslow 1c![]() ![]() |
THF | N Param.: 16.61 sN Param.: 0.68 | ![]() ![]() ![]() | Angew. Chem. Int. Ed. 2012, 51, 10408-10412 10.1002/anie.201204524 |
anion of diethyl 2-(p-anisyl)malonate (in DMSO)![]() ![]() |
DMSO | N Param.: 16.73 sN Param.: 0.91 | ![]() ![]() ![]() | Eur. J. Org. Chem. 2016, , 1841-1848 10.1002/ejoc.201600107 |
anion of (4-cyanophenyl)nitromethane (in DMSO)![]() ![]() |
DMSO | N Param.: 16.96 sN Param.: 0.73 | ![]() ![]() ![]() | J. Org. Chem. 2004, 69, 7565-7576 10.1021/jo048773j |
3-acetyl-2-oxotetrahydro-2H-pyran-3-ide (in DMSO)![]() ![]() |
DMSO | N Param.: 17.00 sN Param.: 0.74 | ![]() ![]() ![]() | Eur. J. Org. Chem. 2015, , 7594-7601 10.1002/ejoc.201501107 |
Desoxy Breslow intermediate 2a![]() ![]() |
THF | N Param.: 17.12 sN Param.: 0.80 | ![]() ![]() ![]() | Angew. Chem. Int. Ed. 2012, 51, 6231-6235 10.1002/anie.201202327 |