A convenient synthesis of .ALPHA.-(2-benzothiazolylthio)alkanoates by cleavage of .BETA.-keto esters with 2-benzothiazolesulfenamides.
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概要
- 論文の詳細を見る
α-(2-Benzothiazolylthio)alkanoates were prepared by the reaction of β-keto esters with 2-(morpholinothio)benzothiazole in refluxing alcohols. Sulfenylating cleavage of α-methoxycarbonylcycloalkanones afforded the corresponding ω-alkoxycarbonyl- and/or ω-carbamoyl-α-(2-benzothiazolylthio)alkanoates.
- 公益社団法人 日本化学会の論文
著者
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Torii Sigeru
Department Of Applied Chemistry Faculty Of Engineering Okayama University
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Tanaka Hideo
Department Of Applied Chemistry Faculty Of Engineering Okayama University
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OKUMOTO Hiroshi
Department of Chemical Technology, College of Science and Industrial Technology, Kurashiki University of Science and Arts
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Okumoto Hiroshi
Department of Industrial Chemistry, School of Engineering, Okayama University
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