Behaviour of S-substituted cysteine sulfoxide under acidolytical deprotecting conditions.
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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.
収録刊行物
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- CHEMICAL & PHARMACEUTICAL BULLETIN
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CHEMICAL & PHARMACEUTICAL BULLETIN 27 (4), 1060-1061, 1979
公益社団法人 日本薬学会
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詳細情報 詳細情報について
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- CRID
- 1390001204172577024
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- NII論文ID
- 110003662295
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- NII書誌ID
- AA00602100
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- ISSN
- 13475223
- 00092363
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- 本文言語コード
- en
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- データソース種別
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- JaLC
- Crossref
- CiNii Articles
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- 抄録ライセンスフラグ
- 使用不可