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Autoxidation of polysubstituted isoindoles. Part II. Products from 1,3-diphenyl- and 1,2,3-triphenyl-isoindoles

✍ Scribed by Ahmed, Munir; Kricka, Larry J.; Vernon, John M.


Book ID
121276420
Publisher
Royal Society of Chemistry
Year
1975
Weight
730 KB
Volume
1
Category
Article
ISSN
1472-7781

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## 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