Transformation of isoxazolines into aziridines by lithium aluminum hydride reduction
- 1 January 1968
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 9 (55) , 5759-5762
- https://doi.org/10.1016/s0040-4039(00)76343-x
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
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- Stereochemistry of aziridine formation by reduction of oximes with lithium aluminum hydride on aralkyl alkyl ketoximes and their tosylatesTetrahedron, 1968
- Aziridine formation by lithium aluminum hydride reduction of oximesTetrahedron, 1968
- Stereochemistry of aziridine formation by lithium aluminum hydride reduction of ketoximes of bridged ring systems. On benzobicyclo[3.2.1]octenone oximesTetrahedron Letters, 1968
- Aziridine formation by lithium aluminum hydride reduction of ketoximes of bridged ring systemsTetrahedron, 1968
- Formation of aziridines by lithium aluminum hydride reduction of ketoximesTetrahedron Letters, 1965
- 163. Reduction of phenyl vinyl ketoxime with lithium aluminium hydrideJournal of the Chemical Society, 1965
- The Chemistry of the 2-Isoxazolines: Reductive CleavagesJournal of the American Chemical Society, 1957