Activation of Weak Organic Bases. VI. The Alkylation of Thiol Esters by Triethyloxonium Salt and Diethoxycarbonium Salt (HC^^+(OC_2H_5)_2,S^^-bCl_6)
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概要
- 論文の詳細を見る
The alkylation of thiol esters with effective alkylating reagents was studied. It was found that the process which afford products was in most cases thermodynamically controlled, which establishes the high susceptibility of the divalent sulfur in thiol esters to the alkylating reagents.
- 公益社団法人日本薬学会の論文
- 1971-10-25
著者
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塩沢 真理子
Faculty Of Pharmaceutical Sciences Hokkaido University
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伴 義雄
Faculty of Pharmaceutical Sciences, School of Medicine, Hokkaido University
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大石 武
Faculty Of Engineering Yokohama National University:(present Address)meiji College Of Pharmacy
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森 美和子
北大・薬
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伴 義雄
東邦大・薬
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伴 義雄
Faculty Of Pharmaceutical Sciences Hokkaido University
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大石 武
北大・薬:(現)理化学研究所
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森 美和子
Faculty of Pharmaceutical Sciences, Hokkaido University
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