Direct Conversion of a Benzylic Hydroxy Group into a Selenenyl Group Using the Phenyl Trimethylsilyl Selenide-Aluminum Bromide Combination

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概要

• 論文の詳細を見る

• A new reagent system, phenyl trimethylsilyl selenide-aluminum bromide, was developed for the direct conversion of various benzylic hydroxy groups into a selenenyl group. Treatment of cinnamyl alcohol with this reagent system yielded 3,4-dihydro-4-phenyl-2H-1-benzoselenin via a [3,3]-sigmatropic rearrangement of the intermediate cinnamyl phenyl selenide.

• 公益社団法人日本薬学会の論文
• 1998-08-15

著者

• 原山 尚

  Faculty Of Pharmaceutical Sciences Kyoto University

• ABE Hitoshi

  Faculty of Pharmaceutical Sciences, Okayama University

• HARAYAMA Takashi

  Faculty of Pharmaceutical Sciences, Okayama University

• YAMASAKI Akira

  Faculty of Pharmaceutical Sciences, Okayama University

• Abe H

  Graduate School Of Sci. And Engineering Univ. Of Toyama

• Yamasaki A

  Faculty Of Pharmaceutical Sciences Okayama University

• Harayama Takashi

  Faculty Of Pharmaceutical Sciences Okayama University

• Abe Hitoshi

  Univ. Toyama Toyama Jpn

• Abe Hitoshi

  Faculty Of Pharmaceutical Sciences Okayama University:advanced Science Research Center Okayama Unive

• Abe Hitoshi

  Faculty Of Pharmaceutical Sciences Okayama University

• Yamasaki Akira

  Faculty Of Pharmaceutical Sciences Okayama University

• Harayama Takashi

  Faculty of Pharmaceutical Sciences at Kagawa Campus, Tokushima Bunri University

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