Stereochimie de la reduction de cyclohexenones oximes α,β-insaturees par li Al H4
- 31 December 1973
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 14 (42) , 4151-4154
- https://doi.org/10.1016/s0040-4039(01)87135-5
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Synthesis of Some Epiminocyclohexanes by Hydride Reduction of α,β-Unsaturated Cyclohexanone Oximes and the Pyrolytic cis-Elimination of N-AcetylepiminocyclohexanesCanadian Journal of Chemistry, 1973
- Beckmann rearrangement of α,β-unsaturated ketoximes in cyclic systemsTetrahedron, 1971
- Conversion of 2-isoxazolines into aziridines by lithium aluminum hydride reductionTetrahedron, 1970
- SYNTHESIS OF AZIRIDINES BY REDUCTION OF OXIMES WITH LITHIUM ALUMINUM HYDRIDE A REVIEWOrganic Preparations and Procedures, 1969
- Aziridine formation by lithium aluminum hydride reduction of ketoximes of bridged ring systemsTetrahedron, 1968
- 163. Reduction of phenyl vinyl ketoxime with lithium aluminium hydrideJournal of the Chemical Society, 1965
- 641. Aza-steroids. Part VIII. 7a-aza-B-homo-5α-cholestane and 7a-aza-B-homocholest-5-eneJournal of the Chemical Society, 1964
- ELECTRICAL POLARIZATION OF TETRAMETHYLCYCLOBUTANESCanadian Journal of Chemistry, 1963