## 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
✦ LIBER ✦
ChemInform Abstract: Unanticipated Products from Reductive and Oxidative Cleavages of 1-Substituted 3,3-Diphenyl-1′-methylspiro[azetidine-2,3′-indoline]-2′,4-diones.
✍ Scribed by Girija S. Singh; Patrick M. Luntha
- Book ID
- 112043123
- Publisher
- John Wiley and Sons
- Year
- 2012
- Weight
- 27 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0931-7597
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
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