Bisbenzylisoquinoline Alkaloids and Related Compounds. XI. Total Synthesis of Stereoisomeric Mixture of Magnoline

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概要

• 論文の詳細を見る

• The diamide (IX) was prepared by Schotten-Baumann reaction of 2-(3-methoxy-4-hydroxyphenyl) ethylamine with the diacid chloride (V), followed by ethoxycarbonylation. Cyclization gave the bisdihydroisoquinoline (XI), the dimethiodide of which, on reduction, gave a stereoisomeric mixture of magnoline or berbamunine (I).

• 社団法人日本薬学会の論文
• 1967-01-25

著者

• 亀谷 哲治

  Pharmaceutical Institute, Tohoku University School of Medicine

• 加納 慎蔵

  Tokyo College of Pharmacy

• 柳瀬 良文

  Pharmaceutical Institute, Tohoku University School of Medicine

• 加納 慎蔵

  Pharmaceutical Institute, Tohoku University School of Medicine

• 桜井 邦好

  Pharmaceutical Institute, Tohoku University School of Medicine

• 亀谷 哲治

  Pharmaceutical Institute Medical Faculty University Of Osaka

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