The Ring Transformation of 1,2,3-Triazines

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概要

• 論文の詳細を見る

• Monocyclic 1,2,3-triazines reacted with electron rich dienophiles to give pyridines and pyridazines. 4,6-Disubstituted 1,2,3-triazine was denitrogenated to the azete intermediate, which afforded isomeric pyridines. 2,5-Dihydrotriazines were oxidized by m-chloroperbenzoic acid to give 1,2,3-triazoles. Ring transformations of other triazine derivatives are also reported.

• 社団法人日本薬学会の論文
• 1990-08-25

著者

• 山口 健太郎

  School of Pharmaceutical Sciences, Showa University

• 大沢 昭緒

  School of Pharmaceutical Sciences, Showa University

• 山口 健太郎

  School Of Pharmaceutical Sciences Showa University

• 伊藤 喬

  昭和大学薬学部薬化学教室

• 伊藤 喬

  School of Pharmaceutical Sciences, Showa University

• 岡田 真弥子

  School of Pharmaceutical Sciences, Showa University

• 永田 和弘

  School of Pharmaceutical Sciences, Showa University

• 大沢 昭緒

  School Of Pharmaceutical Sciences Showa University

• Nagata K

  School Of Pharmaceutical Sciences Showa University

• 岡田 真弥子

  School Of Pharmaceutical Sciences Showa University

• 永田 和弘

  School Of Pharmaceutical Sciences Showa University

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