N-Nucleophiles
| Name | Solvent |
Reactivity Parameters |
Classification |
Reference (title or year) |
|---|---|---|---|---|
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 |
|
(F)2-HBTM (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 |
|
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 |
|
O-DHPB (in CH2Cl2) ![]() |
dichloromethane | N Param.: 13.31 sN Param.: 0.69 |
Angew. Chem. Int. Ed. 2025, 64, e202514865 10.1002/anie.202514865 |
|
O-HyperBTM (in CH2Cl2) ![]() |
dichloromethane | N Param.: 13.01 sN Param.: 0.73 |
Angew. Chem. Int. Ed. 2025, 64, e202514865 10.1002/anie.202514865 |

