Intramolecular Photoreactions of Phthalimide-Alkene Systems. Oxetane Formation of N-(ω-Indol-3-ylalkyl)phthalimides
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概要
- 論文の詳細を見る
Upon irradiation in acetone, N-(ω-indol-3-ylalkyl)phthalimides (1,n=2-5) underwent intramolecular Paterno-Buchi reaction to give oxeto[2,3-b]indoles or their ring-opening products. However, N-(ω-indol-2-ylalkyl)phthalimides (9,n=2,3) yielded not the oxetane, but the N-deacetylated compounds.
- 1988-08-25
著者
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金岡 祐一
Faculty of Pharmaceutical Sciences, Hokkaido University
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武智 春子
Faculty Of Pharmaceutical Sciences Higashi-nippon-gakuen University
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金岡 祐一
Toyama Women's College
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町田 實
Faculty of Pharmaceutical Sciences, Higashi Nippon Gakuen University
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町田 實
Faculty Of Pharmaceutical Sciences Higashi-nippon-gakuen University
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