Synthetic Studies on Lycoricidine and Related Compounds. I. Synthesis of 4aH-r, 2H-cis, 2-Hydroxy-8,9-methylenedioxy-2,3,4,4a-tetrahydro-6 (5H)-phenanthridone
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概要
- 論文の詳細を見る
4aH-r, 2H-cis, 2-Hydroxy-2,3,4,4a-tetrahydro-8,9-methylenedioxy-6 (5H)-phenanthridone, which was an important compound lacking two hydroxyl groups at 3-and 4-position in the structure of lycoricidine, was synthesized and configuration of the hydroxyl group was comfirmed to be α-quassi-axial on the basis of NMR data. A new lactam cyclization technique using borontrifluoride etherate on the course from phenethyl isocyanates to the corresponding lactams was examined.
- 公益社団法人日本薬学会の論文
- 1976-12-25
著者
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太田 俊作
Kyoto Pharmaceutical University
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木本 正七郎
Kyoto College of Pharmacy
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太田 俊作
Kyoto College Of Pharmacy
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