Selective Reduction of Peptide-ester Groups in Aqueous Solution III. Valine and Proline Esters
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概要
- 論文の詳細を見る
The selective reduction of peptide-ester groups in aqueous solution with sodium borohydride was examined. For the sterically hindered esters, which resist to the reduction, in particular N-acetylglycyl-L-valine methyl ester and N-acetylglycyl-L-proline methyl ester, the reduction was examined in detail under various conditions. Consequently, these esters could be reduced almost quantitatively to the corresponding alcohols, indicating the potential utility in protein chemistry.
- 公益社団法人日本薬学会の論文
- 1972-05-25
著者
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米光 宰
Faculty of Pharmaceutical Sciences, Hokkaido University
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米光 宰
北海道大学薬学部
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米光 宰
Faculty Of Pharmaceutical Sciences Hokkaido University
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浜田 辰夫
Faculty of Pharmaceutical Sciences, Hokkaido University
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浜田 辰夫
北大薬
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米光 宰
北大 薬
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鈴木 美津江
Faculty of Pharmaceutical Sciences, Hokkaido University
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鈴木 美津江
Faculty Of Pharmaceutical Sciences Hokkaido University
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