Studies on the Syntheses of Heterocyclic Compounds. CDLXXXVII. Photolytic Synthesis and Rearrangement of Proerythrinadienones
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概要
- 論文の詳細を見る
Photolysis of the 1-(2-bromobenzyl)-1,2,3,4-tetrahydro-7-hydroxyisoquinolines (VII, VIII, and X) gave the proerythrinadienones (XIII, XIV, and XV), which would be key precursors for several isoquinoline alkaloids. The acidic treatment of these dienones and the corresponding dienols (XXXII) was investigated under several conditions.
- 社団法人日本薬学会の論文
- 1972-08-25
著者
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本多 利雄
Institute Of Medicinal Chemistry Hoshi University
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井原 正隆
東北大院薬
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亀谷 哲治
Pharmaceutical Institute, Tohoku University School of Medicine
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高橋 恵一
Pharmaceutical Research Laboratories Kyowa Hakko Kogyo Co. Ltd.
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高橋 恵一
Pharmaceutical Institute Tohoku University
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福本 圭一郎
東北大・薬
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福本 圭一郎
Pharmaceutical Institute, Tohoku University
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井原 正隆
Pharmaceutical Institute, Tohoku University
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井原 正隆
東北大薬
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井原 正隆
東北大学薬学部
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本多 利雄
Pharmaceutical Institute, Tohoku University
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亀谷 哲治
Pharmaceutical Institute Medical Faculty University Of Osaka
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福本 圭一郎
Pharmaceutical Institute Tohoku University School Of Medicine
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