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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作  者:Chen-Hao Ding Jian-Lian Dong Li-Si-Han Yu Jian-Wu Xie 

机构地区:[1]Department of Chemistry and Life science, Zhejiang Normal University, Jinhua 321004, China

出  处:《Chinese Chemical Letters》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)

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.

关 键 词:Dihydrothiophenes Organocatalysis 1 3-Dicarbonyl compounds Thioamides Nitrostyrenes 

分 类 号:O626.12[理学—有机化学]

 

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