Behaviour of S-Substituted Cysteine Sulfoxide under Acidolytical Deprotecting Conditions

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概要

• 論文の詳細を見る

• Treatment of S-p-methoxybenzylcysteine sulfoxide with hydrogen fluoride or methanesulfonic acid in the presence of anisole afforded S-p-methoxyphenylcysteine as a major product, while S-benzylcysteine sulfoxide resisted to the action of these deprotecting reagents in peptide synthesis. Thiophenol was found to be a powerful reducing reagent of the sulfoxides.

• 公益社団法人日本薬学会の論文
• 1979-04-25

著者

• 藤井 信孝

  Faculty of Pharmaceutical Sciences, Kyoto University

• 矢島 治明

  Faculty of Pharmaceutical Sciences, Kyoto University

• 入江 寛

  長崎大薬

• 船越 奨

  Faculty of Pharmaceutical Sciences

• 赤路 健一

  Faculty of Pharmaceutical Sciences

• 入江 寛

  長崎大学薬学部

• 入江 寛

  Faculty Of Pharmaceutical Sciences Kyoto University

• 矢島 治明

  Faculty Of Pharmaceutical Sciences Kyoto University

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