Nucleophiles
Name | Solvent |
Reactivity Parameters |
Classification |
Reference (title or year) |
---|---|---|---|---|
3-methylpyridine (in CH2Cl2)![]() ![]() |
dichloromethane | N Param.: 10.90 sN Param.: 0.93 | ![]() ![]() ![]() | J. Phys. Org. Chem. 2016, 29, 759-767 10.1002/poc.3580 |
1-methyl-2-phenylpyrrolidine (in CH2Cl2)![]() ![]() |
dichloromethane | N Param.: 16.80 sN Param.: 0.49 | ![]() ![]() ![]() | J. Phys. Org. Chem. 2016, 29, 759-767 10.1002/poc.3580 |
4-(morpholino)pyridine (in CH2Cl2)![]() ![]() |
dichloromethane | N Param.: 14.59 sN Param.: 0.69 | ![]() ![]() ![]() | Eur. J. Org. Chem. 2016, , 4050-4058 10.1002/ejoc.201600572 |
Cp2Zr(Me)2 - Dimethylzirconocene![]() ![]() |
dichloromethane | N Param.: 4.35 sN Param.: 1.09 | ![]() ![]() ![]() | Chem. Eur. J. 2016, 22, 11196-11200 10.1002/chem.201602452 |
Cp2Zr(CH2Ph)2 - Dibenzylzirconocene![]() ![]() |
dichloromethane | N Param.: 5.10 sN Param.: 1.03 | ![]() ![]() ![]() | Chem. Eur. J. 2016, 22, 11196-11200 10.1002/chem.201602452 |
Cp2Ti(CH2Ph)2 - Dibenzyltitanocene![]() ![]() |
dichloromethane | N Param.: 4.38 sN Param.: 1.00 | ![]() | Chem. Eur. J. 2016, 22, 11196-11200 10.1002/chem.201602452 |
(Cp*)2Zr(Me)2 - Dimethyl-bis(pentamethylcyclopentadienyl)zirconium![]() ![]() |
dichloromethane | N Param.: 5.49 sN Param.: 1.06 | ![]() ![]() ![]() | Chem. Eur. J. 2016, 22, 11196-11200 10.1002/chem.201602452 |
Dimethyl 1,1'-isopropylidenezirconocene![]() ![]() |
dichloromethane | N Param.: 5.20 sN Param.: 1.00 | ![]() | Chem. Eur. J. 2016, 22, 11196-11200 10.1002/chem.201602452 |
Dimethyl bis(indenyl)zirconium(IV)![]() ![]() |
dichloromethane | N Param.: 6.89 sN Param.: 1.00 | ![]() | Chem. Eur. J. 2016, 22, 11196-11200 10.1002/chem.201602452 |
Meldrum's acid iodonium ylide (in CH2Cl2)![]() ![]() |
dichloromethane | N Param.: 4.36 sN Param.: 1.06 | ![]() ![]() ![]() | J. Am. Chem. Soc. 2016, 138, 10304-10313 10.1021/jacs.6b05768 |
Dimedone iodonium ylide (in CH2Cl2)![]() ![]() |
dichloromethane | N Param.: 6.18 sN Param.: 0.81 | ![]() ![]() ![]() | J. Am. Chem. Soc. 2016, 138, 10304-10313 10.1021/jacs.6b05768 |
N,N-Dimethylbarbituric acid iodonium ylide (in CHCl2)![]() ![]() |
dichloromethane | N Param.: 7.98 sN Param.: 0.71 | ![]() ![]() ![]() | J. Am. Chem. Soc. 2016, 138, 10304-10313 10.1021/jacs.6b05768 |
6-methyl-3-(phenyl-l3-iodanylidene)dihydro-2H-pyran-2,4(3H)-dione (in CH2Cl2)![]() ![]() |
dichloromethane | N Param.: 4.67 sN Param.: 0.92 | ![]() ![]() ![]() | J. Am. Chem. Soc. 2016, 138, 10304-10313 10.1021/jacs.6b05768 |
ditert-butyl-phenylphosphane![]() ![]() |
dichloromethane | N Param.: 12.40 sN Param.: 0.55 | ![]() | Chem. Eur. J. 2017, 23, 7422-7427 10.1002/chem.201701080 |
tris(2,6-dimethoxyphenyl)phosphane![]() ![]() |
dichloromethane | N Param.: 15.19 sN Param.: 0.88 | ![]() | Chem. Eur. J. 2017, 23, 7422-7427 10.1002/chem.201701080 |
tris(2,4-dimethylphenyl)phosphane![]() ![]() |
dichloromethane | N Param.: 14.88 sN Param.: 0.41 | ![]() | Chem. Eur. J. 2017, 23, 7422-7427 10.1002/chem.201701080 |
tris(2-methoxyphenyl)phosphane![]() ![]() |
dichloromethane | N Param.: 14.26 sN Param.: 0.73 | ![]() | Chem. Eur. J. 2017, 23, 7422-7427 10.1002/chem.201701080 |
tris(2-methylphenyl)phosphane![]() ![]() |
dichloromethane | N Param.: 8.56 sN Param.: 0.70 | ![]() | Chem. Eur. J. 2017, 23, 7422-7427 10.1002/chem.201701080 |
4,4,5,5-tetramethyl-2-prop-2-enyl-1,3,2-dioxaborolane (in CH2Cl2)![]() ![]() |
dichloromethane | N Param.: -0.64 sN Param.: 1.10 | ![]() ![]() ![]() | J. Am. Chem. Soc. 2017, 139, 15324-15327 10.1021/jacs.7b10240 |
(p-nitrophenyl)diazomethane![]() ![]() |
dichloromethane | N Param.: 7.17 sN Param.: 0.83 | ![]() ![]() ![]() | J. Am. Chem. Soc. 2018, 140, 16758-16772 10.1021/jacs.8b09995 |
(p-cyanophenyl)diazomethane![]() ![]() |
dichloromethane | N Param.: 7.66 sN Param.: 0.80 | ![]() ![]() ![]() | J. Am. Chem. Soc. 2018, 140, 16758-16772 10.1021/jacs.8b09995 |
(p-bromophenyl)diazomethane![]() ![]() |
dichloromethane | N Param.: 8.87 sN Param.: 0.82 | ![]() ![]() ![]() | J. Am. Chem. Soc. 2018, 140, 16758-16772 10.1021/jacs.8b09995 |
dimethylsulfide (in CH2Cl2)![]() ![]() |
dichloromethane | N Param.: 12.32 sN Param.: 0.72 | ![]() ![]() | Chem. Eur. J. 2021, 21, 11367-11376 10.1002/chem.202100977 |
dimethylselenide (in CH2Cl2)![]() ![]() |
dichloromethane | N Param.: 12.60 sN Param.: 0.72 | ![]() | Chem. Eur. J. 2021, 21, 11367-11376 10.1002/chem.202100977 |
dibutylsulfide (in CH2Cl2)![]() ![]() |
dichloromethane | N Param.: 11.86 sN Param.: 0.74 | ![]() ![]() | Chem. Eur. J. 2021, 21, 11367-11376 10.1002/chem.202100977 |
tetrahydrothiophene (in CH2Cl2)![]() ![]() |
dichloromethane | N Param.: 13.10 sN Param.: 0.72 | ![]() | Chem. Eur. J. 2021, 21, 11367-11376 10.1002/chem.202100977 |
tetrahydrothiopyran (in CH2Cl2)![]() ![]() |
dichloromethane | N Param.: 11.94 sN Param.: 0.75 | ![]() ![]() | Chem. Eur. J. 2021, 21, 11367-11376 10.1002/chem.202100977 |
3-diazoindolin-2-one![]() ![]() |
dichloromethane | N Param.: 3.16 sN Param.: 1.03 | ![]() ![]() ![]() | Eur. J. Org. Chem. 2023, 26, e202300005 10.1002/ejoc.202300005 |
2-diazoindan-1-one![]() ![]() |
dichloromethane | N Param.: 5.61 sN Param.: 0.65 | ![]() ![]() ![]() | Eur. J. Org. Chem. 2023, 26, e202300005 10.1002/ejoc.202300005 |
2-diazocyclohexanone![]() ![]() |
dichloromethane | N Param.: 3.44 sN Param.: 0.83 | ![]() ![]() ![]() | Eur. J. Org. Chem. 2023, 26, e202300005 10.1002/ejoc.202300005 |
2-diazo-1-tetralone![]() ![]() |
dichloromethane | N Param.: 3.51 sN Param.: 0.86 | ![]() ![]() ![]() | Eur. J. Org. Chem. 2023, 26, e202300005 10.1002/ejoc.202300005 |
2-diazoindandione![]() ![]() |
dichloromethane | N Param.: 0.16 sN Param.: 0.86 | ![]() ![]() ![]() | Eur. J. Org. Chem. 2023, 26, e202300005 10.1002/ejoc.202300005 |
2-diazo-1-benzosuberone![]() ![]() |
dichloromethane | N Param.: 2.72 sN Param.: 0.96 | ![]() ![]() ![]() | Eur. J. Org. Chem. 2023, 26, e202300005 10.1002/ejoc.202300005 |
2-diazobenzothiophen-3(2H)-one![]() ![]() |
dichloromethane | N Param.: 0.40 sN Param.: 0.93 | ![]() ![]() ![]() | Eur. J. Org. Chem. 2023, 26, e202300005 10.1002/ejoc.202300005 |
2-((2,2,5,5-tetramethyl-1-styryl-2,5-dihydro-1H-imidazol-4-yl)thio)acetonitrile (in CH2Cl2)![]() ![]() |
dichloromethane | N Param.: 7.06 sN Param.: 1.11 | ![]() ![]() ![]() | Chem. Commun. 2023, 59, 8091-8084 10.1039/d3cc01912h |
diazocyclopentadiene (in CH2Cl2)![]() ![]() |
dichloromethane | N Param.: 4.84 sN Param.: 1.06 | ![]() ![]() ![]() | Synthesis 2023, 55, 354-358 10.1055/s-0041-1737327 |
(E)-4-(ethylthio)-2,2,5,5-tetramethyl-1-styryl-2,5-dihydro-1H-imidazole (in CH2Cl2)![]() ![]() |
dichloromethane | N Param.: 8.13 sN Param.: 0.97 | ![]() ![]() ![]() | Chem. Eur. J. 2024, 30, e202302764 10.1002/chem.202302764 |
(E)-4-(benzylthio)-2,2,5,5-tetramethyl-1-styryl-2,5-dihydro-1H-imidazole (in CH2Cl2)![]() ![]() |
dichloromethane | N Param.: 7.99 sN Param.: 0.98 | ![]() ![]() ![]() | Chem. Eur. J. 2024, 30, e202302764 10.1002/chem.202302764 |
(S)-3,3-difluoro-2-phenyl-3,4-dihydro-2H-benzo[4,5]thiazolo[3,2-a]pyrimidine (in CH2Cl2)![]() ![]() |
dichloromethane | N Param.: 10.83 sN Param.: 0.80 | ![]() ![]() ![]() | ARKIVOC 2024, (4), 202312093 10.24820/ark.5550190[...] |
2-methylpyridine (in CH2Cl2)![]() ![]() |
dichloromethane | N Param.: 10.52 sN Param.: 0.78 | ![]() ![]() ![]() | Synthesis 2017, 49, 3495-3504 10.1055/s-0036-1590504 |
2,6-dimethylpyridine (in CH2Cl2)![]() ![]() |
dichloromethane | N Param.: 9.87 sN Param.: 0.68 | ![]() ![]() ![]() | Synthesis 2017, 49, 3495-3504 10.1055/s-0036-1590504 |
2,4,6-trimethylpyridine (in CH2Cl2)![]() ![]() |
dichloromethane | N Param.: 9.34 sN Param.: 0.71 | ![]() ![]() ![]() | Synthesis 2017, 49, 3495-3504 10.1055/s-0036-1590504 |
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 |
benzoate (in 90AN10W)![]() ![]() |
aq MeCN | N Param.: 11.30 sN Param.: 0.72 | ![]() ![]() | J. Am. Chem. Soc. 2008, 130, 3012-3022 10.1021/ja0765464 |
acetate (in 90A10W)![]() ![]() |
aq acetone | N Param.: 12.71 sN Param.: 0.68 | ![]() ![]() ![]() | J. Am. Chem. Soc. 2008, 130, 3012-3022 10.1021/ja0765464 |
acetate (in 80A20W)![]() ![]() |
aq acetone | N Param.: 12.50 sN Param.: 0.60 | ![]() ![]() | J. Am. Chem. Soc. 2008, 130, 3012-3022 10.1021/ja0765464 |
p-nitrobenzoate (in acetone)![]() ![]() |
acetone | N Param.: 18.74 sN Param.: 0.68 | ![]() ![]() ![]() | J. Am. Chem. Soc. 2008, 130, 3012-3022 10.1021/ja0765464 |