The Stereochemistry of Hydrastine, Narcotine, Ophiocarpine, and their Derivatives. II. Absolute Configuration of Narcotine and their Derivatives

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概要

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• The natural l-α-narcotine (Iα) and its epimer l-β-narcotine (Iβ) were stereospecifically converted into 1-(2-methyl-3,4-dimethoxybenzyl)-6,7-methylenedioxy-1,2,3,4-tetrahydroisoquinoline (IV) and (-)-1-methoxycanadine (X), respectively. According to these results, the absolute configuration of Iα and Iβ were established as (αS : 1R) and (αS : 1R), respectively.

• 公益社団法人日本薬学会の論文
• 1964-09-25

著者

• 谷 英郎

  Kowa Chemical Laboratories Kowa Co. Ltd.

• 太田 道敏

  Kowa Chemical Laboratories

• 両角 積子

  Kowa Chemical Laboratories, Kowa Co., Ltd.

• 小平 早智子

  Kowa Chemical Laboratories, Kowa Co., Ltd.

• 小平 早智子

  Kowa Chemical Laboratories Kowa Co. Ltd.

• 両角 積子

  Kowa Chemical Laboratories Kowa Co. Ltd.

• 太田 道敏

  Kowa Chemical Laboratories Kowa Co. Ltd.

関連論文

• Aconitum-Alkaloide. III. : Uber die Konstitution des Ignavins. (1).
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• Studies on Abietic Acid Derivatives. II. Deisopropylation of Dehydroabietic Acid. (2).
• Studies on Abietic Acid Derivatives. I. Deisopropylation of Dehydroabietic Acid. (1).
• The Stereochemistry of Hydrastine, Narcotine, Ophiocarpine, and their Derivatives. II. Absolute Configuration of Narcotine and their Derivatives
• The Stereochemistry of Hydrastine, Narcotine, Ophiocarpine, and their Derivatives. I. Absolute Configuration of Hydrastine and Ophiocarpine
• The Reaction of N-Alkoxypyridinium Derivatives. (2)
• Synthesis of 2- and 4-Cyanopyridines
• Studies on Abietic Acid Derivatives. III. Synthesis of Fluorenone Derivatives.
• アザジテルペノイド(第4報)1-Methoxycarbonyl-1,12-dimethyl-7-amino-1,2,3,4,9,10,11,12-octahydrophenanthreneの合成

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