Studies on Tetrahydroisoquinolines. XXIX. : Reaction of 7-Acetoxy-1,2,3,4,6,7-hexahydro-1-(2-(3',4'-dimethoxy- or 3',4'-methylenedioxyphenyl)ethyl)-7-methoxy-2-methyl-6-oxo-isoquinoline (о-Quinol Acetate) with Acetic Anhydride in the Presence of Acid(Orga
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概要
- 論文の詳細を見る
Treatment of о-quinol acetates (5a, b) of 1,2,3,4-tetrahydro-1-phenethylisoquinolin-6-ols (6a, b) with acetic anhydride in the presence of an acid (concentrated H_2SO_4, BF_3・ Et_2O or CF_3COOH) gave 2-acetoxyhomoaporphines (4a, b) and/or aldehyde-amides (7a, b), and the ratio of the products was strongly dependent on the choice of the acid and the solvent. A mechanistic pathway is proposed.
- 社団法人日本薬学会の論文
- 1987-09-25
著者
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Kikuchi K
Univ. Tokyo Tokyo Jpn
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HOSHINO OSAMU
Faculty of Pharmaceutical Sciences, Science University of Tokyo
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KIKUCHI KYOKO
Faculty of Pharmaceutical Sciences, Science University of Tokyo
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OGOSE HIDETO
Faculty of Pharmaceutical Sciences, Science University of Tokyo
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UMEZAWA BUNSUKE
Faculty of Pharmaceutical Sciences, Science University of Tokyo
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IITAKA YOICHI
Faculty of Pharmaceutical Sciences, Univesity of Tokyo
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Ogose Hideto
Faculty Of Pharmaceutical Sciences Science University Of Tokyo
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Iitaka Yoichi
Faculty Of Pharmaceutical Sciences Univesity Of Tokyo
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Iitaka Yoichi
Faculty Of Medicine Teikyo University
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Hoshino Osamu
Faculty Of Pharmaceutical Sciences Science University Of Tokyo
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Kikuchi Kyoko
Faculty Of Pharmaceutical Sciences Science University Of Tokyo
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Umezawa B
Science Univ. Tokyo Tokyo Jpn
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Umezawa Bunsuke
Faculty Of Pharmaceutical Sciences Science University Of Tokyo
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