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) |
---|---|---|---|---|
![]() trifluoroacetamide anion (in DMSO) | DMSO | N Parameter: 15.81 sN Parameter: 0.64 | ![]() ![]() ![]() | 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 |
![]() saccharin anion (in MeCN) | MeCN | N Parameter: 10.78 sN Parameter: 0.89 | ![]() ![]() ![]() | 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 |
![]() 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 |
![]() 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 |
![]() methanesulfonamide anion (in DMSO) | DMSO | N Parameter: 18.61 sN Parameter: 0.53 | ![]() ![]() ![]() | 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 |
![]() hydantoin anion (in DMSO) | DMSO | N Parameter: 17.52 sN Parameter: 0.55 | ![]() ![]() ![]() | 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 |
![]() diacetamide anion (in DMSO) | DMSO | N Parameter: 16.05 sN Parameter: 0.70 | ![]() ![]() ![]() | J. Org. Chem. 2010, 75, 5250-5258 DOI: 10.1021/jo1009883 |
![]() cyanamide anion (in DMSO) | DMSO | N Parameter: 20.33 sN Parameter: 0.64 | ![]() ![]() ![]() | J. Org. Chem. 2010, 75, 5250-5258 DOI: 10.1021/jo1009883 |
![]() 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 |
![]() 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 DMSO) | DMSO | N Parameter: 18.97 sN Parameter: 0.62 | ![]() ![]() ![]() | 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 |
![]() 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 |
![]() 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 DMSO) | DMSO | N Parameter: 19.91 sN Parameter: 0.60 | ![]() ![]() ![]() | J. Am. Chem. Soc. 2010, 132, 15380-15389 DOI: 10.1021/ja106962u |
![]() 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 |
![]() (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 |