Hard Acid and Soft Nucleophile System. VI. A Convenient Synthesis of Alkylthiopolycyclic Aromatics with a Metal Halide and Thiol System

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概要

• 論文の詳細を見る

• On treatment with a metal halide and alkanethiol system, polycyclic aromatics having various substituents such as hydroxy, alkoxy, phenoxy, acetoxy, and halogen were easily converted into alkylthiopolycyclic aromatics in high yields. The chemo and regioselectivity are described for the reaction of disubstituted naphthalenes.

• 公益社団法人日本薬学会の論文
• 1983-02-25

著者

• 野出 学

  Kyoto Pharmaceutical University

• 野出 学

  Institute For Chemical Research Kyoto University

• 堀 均

  Pharmaceutical Institute School Of Medicine Keio University

• 西出 喜代治

  京都薬科大学薬品製造学教室 創薬科学フロンティア研究センター

• 太田 敬一郎

  Institute For Chemical Research Kyoto University

• 稲山 誠一

  Pharmaceutical Institute, School of Medicine, Keio University

• 藤田 栄一

  京都大学化学研究所

• 藤田 栄一

  Osaka University Of Pharmaceutical Sciences

• 藤田 栄一

  Institute for Chemical Research, Kyoto University

• 藤田 栄一

  Institute For Chemical Research Kyoto University

• 稲山 誠一

  Institute Of Oriental Medical Sciences

• 稲山 誠一

  Pharmaceutical Institute School Of Medicine Keio University

• 稲山 誠一

  慶應義塾大学医学部薬化学研究所

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