Chemistry of Cyclotriveratrylene. I. Formation of Cyclotriveratrylene from Veratrylamine N-Tosylates

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概要

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• Acid treatment (60% HClO_4) of veratrylamine N-tosylates (Va-d) as well as condensation of veratrole and formalin or of veratrylalcohol in the presence of strong acids was proved to give cyclotriveratrylene (III) mainly. On the other hand, the similar reaction of Va with various acids in organic solvents was found to afford both III and cyclotetraveratrylene (IV) in moderate yield.

• 社団法人日本薬学会の論文
• 1969-11-25

著者

• 原 博

  Faculty Of Pharmaceutical Sciences Science University Of Tokyo

• 原 博

  東京理科大学薬学部

• 榊原 仁作

  Faculty of Pharmaceutical Sciences, Nagoya City University

• 榊原 仁作

  Faculty Of Pharmaceutical Sciences Science University Of Tokyo

• 星野 修

  Faculty of Pharmaceutical Sciences, Science University of Tokyo

• 梅澤 文輔

  Faculty of Pharmaceutical Sciences, Science University of Tokyo

• 梅沢 文輔

  Faculty of Pharmaceutical Sciences, Science University of Tokyo

• 大山 恵子

  Faculty of Pharmaceutical Sciences, Science University of Tokyo

• 三林 覚

  Faculty of Pharmaceutical Sciences, Science University of Tokyo

• 梅澤 文輔

  Faculty Of Pharmaceutical Sciences Science University Of Tokyo

• 梅沢 文輔

  Faculty Of Pharmaceutical Sciences Science University Of Tokyo

• 星野 修

  Faculty Of Pharmaceutical Sciences Science University Of Tokyo

• 大山 恵子

  Faculty Of Pharmaceutical Sciences Science University Of Tokyo

• 榊原 仁作

  Faculty Of Pharmaceutical Sciences Nagoya City University

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