Amide anions (N reactivity)
For reactivities of structurally related compounds go to: Nucleophiles » N-Nucleophiles
Found 21 Molecules.
| Molecule | Solvent | Reactivity Parameters | Classification | Reference (sort by title or year) |
|---|---|---|---|---|
 (S)-4-benzyl-1,3-oxazolidin-2-one anion (in DMSO) | DMSO | N Parameter: 22.67 sN Parameter: 0.54 |  | J. Org. Chem. 2010, 75, 5250-5258 DOI: 10.1021/jo1009883 |
 1,3-oxazolidin-2-one anion (in DMSO) | DMSO | N Parameter: 22.40 sN Parameter: 0.59 | | J. Org. Chem. 2010, 75, 5250-5258 DOI: 10.1021/jo1009883 |
 2-pyridone anion (in DMSO) | DMSO | N Parameter: 19.91 sN Parameter: 0.60 | | J. Am. Chem. Soc. 2010, 132, 15380-15389 DOI: 10.1021/ja106962u |
 2-pyridone anion (in MeCN) | MeCN | N Parameter: 20.11 sN Parameter: 0.57 | | J. Am. Chem. Soc. 2010, 132, 15380-15389 DOI: 10.1021/ja106962u |
 2-pyridone anion (in water) | water | N Parameter: 12.47 sN Parameter: 0.52 | | J. Am. Chem. Soc. 2010, 132, 15380-15389 DOI: 10.1021/ja106962u |
 4,4-dimethyl-glutarimide anion (in DMSO) | DMSO | N Parameter: 17.52 sN Parameter: 0.63 | | J. Org. Chem. 2010, 75, 5250-5258 DOI: 10.1021/jo1009883 |
 4-pyridone anion (in DMSO) | DMSO | N Parameter: 18.97 sN Parameter: 0.62 | | J. Am. Chem. Soc. 2010, 132, 15380-15389 DOI: 10.1021/ja106962u |
 4-pyridone anion (in MeCN) | MeCN | N Parameter: 20.22 sN Parameter: 0.49 | | J. Am. Chem. Soc. 2010, 132, 15380-15389 DOI: 10.1021/ja106962u |
 4-pyridone anion (in water) | water | N Parameter: 14.76 sN Parameter: 0.48 | | J. Am. Chem. Soc. 2010, 132, 15380-15389 DOI: 10.1021/ja106962u |
 cyanamide anion (in DMSO) | DMSO | N Parameter: 20.33 sN Parameter: 0.64 | | J. Org. Chem. 2010, 75, 5250-5258 DOI: 10.1021/jo1009883 |
 diacetamide anion (in DMSO) | DMSO | N Parameter: 16.05 sN Parameter: 0.70 | | J. Org. Chem. 2010, 75, 5250-5258 DOI: 10.1021/jo1009883 |
 ethyl N-acetylcarbamate anion (in DMSO) | DMSO | N Parameter: 15.99 sN Parameter: 0.70 | | J. Org. Chem. 2010, 75, 5250-5258 DOI: 10.1021/jo1009883 |
 hydantoin anion (in DMSO) | DMSO | N Parameter: 17.52 sN Parameter: 0.55 | | J. Org. Chem. 2010, 75, 5250-5258 DOI: 10.1021/jo1009883 |
 maleimide anion (in DMSO) | DMSO | N Parameter: 14.87 sN Parameter: 0.76 | | J. Org. Chem. 2010, 75, 5250-5258 DOI: 10.1021/jo1009883 |
 methanesulfonamide anion (in DMSO) | DMSO | N Parameter: 18.61 sN Parameter: 0.53 | | J. Org. Chem. 2010, 75, 5250-5258 DOI: 10.1021/jo1009883 |
 N-methyl-trifluoroacetamide anion (in DMSO) | DMSO | N Parameter: 15.70 sN Parameter: 0.71 | | J. Org. Chem. 2010, 75, 5250-5258 DOI: 10.1021/jo1009883 |
 p-toluenesulfonamide anion (in DMSO) | DMSO | N Parameter: 17.14 sN Parameter: 0.60 | | J. Org. Chem. 2010, 75, 5250-5258 DOI: 10.1021/jo1009883 |
 phthalimide anion (in DMSO) | DMSO | N Parameter: 15.52 sN Parameter: 0.67 | | J. Org. Chem. 2010, 75, 5250-5258 DOI: 10.1021/jo1009883 |
 saccharin anion (in MeCN) | MeCN | N Parameter: 10.78 sN Parameter: 0.89 | | J. Org. Chem. 2010, 75, 5250-5258 DOI: 10.1021/jo1009883 |
 succinimide anion (in DMSO) | DMSO | N Parameter: 16.03 sN Parameter: 0.66 | | J. Org. Chem. 2010, 75, 5250-5258 DOI: 10.1021/jo1009883 |
 trifluoroacetamide anion (in DMSO) | DMSO | N Parameter: 15.81 sN Parameter: 0.64 | | J. Org. Chem. 2010, 75, 5250-5258 DOI: 10.1021/jo1009883 |