- Hoch-Campbell Aziridine Synthesis
-
Hoch-Campbell Aziridine Synthesis
J. Hoch, Compt. Rend. 198, 1865 (1934); K. N. Campbell, J. F. McKenna, J. Org. Chem. 4, 198 (1939).
Formation of aziridines by treatment of ketoximes with Grignard reagents and subsequent hydrolysis of the organometallic complex:

K. N. Campbell et al., J. Org. Chem. 8, 99, 103 (1943); 9, 184 (1944); J. P. Freeman, Chem. Rev. 73, 283 (1973); O. C. Dermer, G. E. Ham, Ethylenimine and Other Aziridines (Academic Press, New York, 1969) pp 65-68; E. Y. Takehisa et al., Chem. Pharm. Bull. 24, 1691 (1976); T. Sasaki et al., Heterocycles 11, 235 (1978); G. Alvernhe, A. Laurent, J. Chem. Res. (S) 1978, 28.
Prev: Camps Quinoline Synthesis
Next: Glaser Coupling - 【Back】【Close 】【Print】【Add to favorite 】
- Related information
-
Health and Chemical more >
-
Hot Products
- 179321-49-4 4-N-Boc-aminocyclohexanone
- 106-42-3 1,4-Dimethylbenzene
- 1406-65-1 Chlorophyll
- 959-26-2 TEREPHTHALIC ACID BIS(2-HYDROXYETHYL) ESTER
- 56-17-7 Ethanamine,2,2'-dithiobis-, hydrochloride (1:2)
- 104983-64-4 Matrimid 5218
- 461432-25-7 D-Glucitol, 1,5-anhydro-1-C-[4-chloro-3-[(4-ethoxyphenyl)Methyl]phenyl]-, tetraacetate, (1S)-
- 8008-20-6 Kerosene
- 100001-00-1 1-propionyl-LSD
- 87-89-8 Inositol
- 3380-34-5 Triclosan
- 500695-53-4 2-amino-2-(2,6-dimethylphenyl)acetic Acid


