Unanticipated products from reductive an
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Girija S. Singh; Patrick M. Luntha
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Article
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2011
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Journal of Heterocyclic Chemistry
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English
⚖ 94 KB
## Abstract Titled spiroazetidinones **1a**, **1b** undergo reductive cleavage on treatment with excess lithium aluminum hydride forming 3‐benzhydryl‐1‐methylindole as the main product together with a γ‐amino alcohol depending upon the substituent present on the azetidin‐2‐one ring. Treatment of 1a