Nucleophiles
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« Back Forward » Found 1310 molecules, displaying page 48 of 66 Results per page
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| Name | Solvent |
Reactivity Parameters |
Classification |
Reference (title or year) |
|---|---|---|---|---|
1,3-dimethyl-2-methylene-1,2-dihydropyridine (in DMSO)  |
DMSO | N Param.: 19.91 sN Param.: 0.62 |  | Eur. J. Org. Chem. 2024, 27, e202400373 10.1002/ejoc.202400373 |
1,3-dimethyl-2-methylene-1,2-dihydropyridine (in MeCN) |
MeCN | N Param.: 19.69 sN Param.: 0.61 | | Eur. J. Org. Chem. 2024, 27, e202400373 10.1002/ejoc.202400373 |
1,6-dimethyl-2-methylene-1,2-dihydropyridine (in DMSO) |
DMSO | N Param.: 20.76 sN Param.: 0.60 | | Eur. J. Org. Chem. 2024, 27, e202400373 10.1002/ejoc.202400373 |
1-methyl-2-methylene-3-phenyl-1,2-dihydropyridine (in DMSO) |
DMSO | N Param.: 19.41 sN Param.: 0.61 | | Eur. J. Org. Chem. 2024, 27, e202400373 10.1002/ejoc.202400373 |
1-(4-(tert-butyl)phenyl)-2-methylene-4,6-diphenyl-1,2-dihydropyridine (in DMSO) |
DMSO | N Param.: 19.36 sN Param.: 0.68 | | Eur. J. Org. Chem. 2024, 27, e202400373 10.1002/ejoc.202400373 |
enolate of 3-isochromanone (in DMSO) |
DMSO | N Param.: 25.39 sN Param.: 0.54 | | J. Org. Chem. 2024, 89, 6915-6928 10.1021/acs.joc.4c00277 |
enolate of 2-coumaranone (in DMSO) |
DMSO | N Param.: 19.60 sN Param.: 0.75 | | J. Org. Chem. 2024, 89, 6915-6928 10.1021/acs.joc.4c00277 |
methyl diazoacetate |
dichloromethane | N Param.: 4.68 sN Param.: 0.94 | | J. Am. Chem. Soc. 2023, 145, 7416-7434 10.1021/jacs.2c13872 |
dimethyl diazomalonate |
dichloromethane | N Param.: -1.24 sN Param.: 0.81 | | J. Am. Chem. Soc. 2023, 145, 7416-7434 10.1021/jacs.2c13872 |
pyridin-4-yl((trifluoromethyl)sulfonyl)amide (Ph4P+) (in CH2Cl2) |
dichloromethane | N Param.: 17.88 sN Param.: 0.73 | | J. Am. Chem. Soc. 2025, 147, 5043-5050 10.1021/jacs.4c14825 |
((4-methoxyphenyl)sulfonyl)(pyridin-4-yl)amide (Ph4P+) (in CH2Cl2) |
dichloromethane | N Param.: 19.63 sN Param.: 0.65 | | J. Am. Chem. Soc. 2025, 147, 5043-5050 10.1021/jacs.4c14825 |
pyridin-4-yl((trifluoromethyl)sulfonyl)amide (Ph4P+) (in MeCN) |
MeCN | N Param.: 16.38 sN Param.: 0.60 | | J. Am. Chem. Soc. 2025, 147, 5043-5050 10.1021/jacs.4c14825 |
((4-methoxyphenyl)sulfonyl)(pyridin-4-yl)amide (Ph4P+) (in MeCN) |
MeCN | N Param.: 17.28 sN Param.: 0.65 | | J. Am. Chem. Soc. 2025, 147, 5043-5050 10.1021/jacs.4c14825 |
pyridin-4-yl((4-(trifluoromethyl)phenyl)sulfonyl)amide (Ph4P+) (in MeCN) |
MeCN | N Param.: 19.51 sN Param.: 0.47 | | J. Org. Chem. 2025, 90, 2298-2306 10.1021/acs.joc.4c02668 |
pyridin-4-yl(tosyl)amide (Ph4P+) (in MeCN) |
MeCN | N Param.: 17.19 sN Param.: 0.64 | | J. Org. Chem. 2025, 90, 2298-2306 10.1021/acs.joc.4c02668 |
pyridin-4-yl((trifluoromethyl)sulfonyl)amide (Bu4P+) (in MeCN) |
MeCN | N Param.: 16.48 sN Param.: 0.60 | | J. Org. Chem. 2025, 90, 2298-2306 10.1021/acs.joc.4c02668 |
pyridin-4-yl((trifluoromethyl)sulfonyl)amide (Bu4N+) (in MeCN) |
MeCN | N Param.: 16.68 sN Param.: 0.59 | | J. Org. Chem. 2025, 90, 2298-2306 10.1021/acs.joc.4c02668 |
50% water/50% MeCN (v/v) |
water-MeCN mix | N Param.: 5.05 sN Param.: 0.89 | | J. Am. Chem. Soc. 2004, 126, 5174-5181 10.1021/ja031828z |
(Z)-but-2-ene |
dichloromethane | N Param.: -2.44 sN Param.: 1.09 | | J. Am. Chem. Soc. 2001, 123, 9500-9512 10.1021/ja010890y |
(triisopropylsiloxy)ethene |
dichloromethane | N Param.: 3.44 sN Param.: 0.94 | | J. Am. Chem. Soc. 2001, 123, 9500-9512 10.1021/ja010890y |