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Organocatalytic Domino Michael/cyclization for the synthesis of highly substituted 4, 5-dihydrothiophenes

Organocatalytic Domino Michael/cyclization for the synthesis of highly substituted 4,5-dihydrothiophenes
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摘要 Based on an umpolung strategy, a series of novel full substituted, optically active dihydrothiophenes, which contain several functional groups, such as amine, ester and oxime groups, were obtained via an efficient organocatalytic asymmetric a formal thio[3 + 2]-cyclization of acyclic thioamides with (E)- α-nitrostyrenes. Based on an umpolung strategy, a series of novel full substituted, optically active dihydrothiophenes, which contain several functional groups, such as amine, ester and oxime groups, were obtained via an efficient organocatalytic asymmetric a formal thio[3 + 2]-cyclization of acyclic thioamides with (E)- α-nitrostyrenes.
出处 《Chinese Chemical Letters》 SCIE CAS CSCD 2018年第3期517-520,共4页 中国化学快报(英文版)
基金 provided by National Natural Science Foundation of China(No. 21272214)
关键词 Dihydrothiophenes Organocatalysis 1 3-Dicarbonyl compounds Thioamides Nitrostyrenes Dihydrothiophenes Organocatalysis 1,3-Dicarbonyl compounds Thioamides Nitrostyrenes
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