Diazo Compounds and Hydrazones
For reactivities of structurally related compounds go to: Nucleophiles » C-Nucleophiles
Found 22 Molecules.
Molecule | Solvent | Reactivity Parameters | Classification | Reference (sort by title or year) |
---|---|---|---|---|
diethyl diazomalonate | dichloromethane | N Parameter: -0.35 sN Parameter: 0.93 | Chem. Eur. J. 2003, 9, 4068-4076 DOI: 10.1002/chem.200304913 | |
diazomethane | dichloromethane | N Parameter: 10.48 sN Parameter: 0.78 | Chem. Eur. J. 2003, 9, 4068-4076 DOI: 10.1002/chem.200304913 | |
phenyldiazomethane | dichloromethane | N Parameter: 9.35 sN Parameter: 0.83 | Chem. Eur. J. 2003, 9, 4068-4076 DOI: 10.1002/chem.200304913 | |
(trimethylsilyl)diazomethane | dichloromethane | N Parameter: 8.97 sN Parameter: 0.75 | Chem. Eur. J. 2003, 9, 4068-4076 DOI: 10.1002/chem.200304913 | |
diphenyldiazomethane | dichloromethane | N Parameter: 5.29 sN Parameter: 0.92 | Chem. Eur. J. 2003, 9, 4068-4076 DOI: 10.1002/chem.200304913 | |
ethyl diazoacetate | dichloromethane | N Parameter: 4.91 sN Parameter: 0.95 | Chem. Eur. J. 2003, 9, 4068-4076 DOI: 10.1002/chem.200304913 | |
diazoacetone | dichloromethane | N Parameter: 3.96 sN Parameter: 0.91 | Chem. Eur. J. 2003, 9, 4068-4076 DOI: 10.1002/chem.200304913 | |
1,1-dimethyl-2-methylenehydrazine (in CH2Cl2) | dichloromethane | N Parameter: 6.98 sN Parameter: 0.85 | Angew. Chem. Int. Ed. 2013, 52, 11900-11904 DOI: 10.1002/anie.201305092 | |
N-methylenepyrrolidin-1-amine (in CH2Cl2) | dichloromethane | N Parameter: 7.84 sN Parameter: 0.89 | Angew. Chem. Int. Ed. 2013, 52, 11900-11904 DOI: 10.1002/anie.201305092 | |
(p-nitrophenyl)diazomethane | dichloromethane | N Parameter: 7.17 sN Parameter: 0.83 | J. Am. Chem. Soc. 2018, 140, 16758-16772 DOI: 10.1021/jacs.8b09995 | |
(p-cyanophenyl)diazomethane | dichloromethane | N Parameter: 7.66 sN Parameter: 0.80 | J. Am. Chem. Soc. 2018, 140, 16758-16772 DOI: 10.1021/jacs.8b09995 | |
(p-bromophenyl)diazomethane | dichloromethane | N Parameter: 8.87 sN Parameter: 0.82 | J. Am. Chem. Soc. 2018, 140, 16758-16772 DOI: 10.1021/jacs.8b09995 | |
3-diazoindolin-2-one | dichloromethane | N Parameter: 3.16 sN Parameter: 1.03 | Eur. J. Org. Chem. 2023, 26, e202300005 DOI: 10.1002/ejoc.202300005 | |
2-diazoindan-1-one | dichloromethane | N Parameter: 5.61 sN Parameter: 0.65 | Eur. J. Org. Chem. 2023, 26, e202300005 DOI: 10.1002/ejoc.202300005 | |
2-diazocyclohexanone | dichloromethane | N Parameter: 3.44 sN Parameter: 0.83 | Eur. J. Org. Chem. 2023, 26, e202300005 DOI: 10.1002/ejoc.202300005 | |
2-diazo-1-tetralone | dichloromethane | N Parameter: 3.51 sN Parameter: 0.86 | Eur. J. Org. Chem. 2023, 26, e202300005 DOI: 10.1002/ejoc.202300005 | |
2-diazoindandione | dichloromethane | N Parameter: 0.16 sN Parameter: 0.86 | Eur. J. Org. Chem. 2023, 26, e202300005 DOI: 10.1002/ejoc.202300005 | |
2-diazo-1-benzosuberone | dichloromethane | N Parameter: 2.72 sN Parameter: 0.96 | Eur. J. Org. Chem. 2023, 26, e202300005 DOI: 10.1002/ejoc.202300005 | |
2-diazobenzothiophen-3(2H)-one | dichloromethane | N Parameter: 0.40 sN Parameter: 0.93 | Eur. J. Org. Chem. 2023, 26, e202300005 DOI: 10.1002/ejoc.202300005 | |
diazocyclopentadiene (in CH2Cl2) | dichloromethane | N Parameter: 4.84 sN Parameter: 1.06 | Synthesis 2023, 55, 354-358 DOI: 10.1055/s-0041-1737327 | |
methyl diazoacetate | dichloromethane | N Parameter: 4.68 sN Parameter: 0.94 | J. Am. Chem. Soc. 2023, 145, 7416-7434 DOI: 10.1021/jacs.2c13872 | |
dimethyl diazomalonate | dichloromethane | N Parameter: -1.24 sN Parameter: 0.81 | Angew. Chem. Int. Ed. Engl. 1994, 33, 938-957 DOI: 10.1002/anie.199409381 |