详细信息

Remote regioselective organocatalytic asymmetric [3+2] cycloaddition of N-2,2,2-trifluoroethyl isatin ketimines with cyclic 2,4-dienones    

文献类型:期刊文献

中文题名:Remote regioselective organocatalytic asymmetric [3+2] cycloaddition of N-2,2,2-trifluoroethyl isatin ketimines with cyclic 2,4-dienones

英文题名:Remote regioselective organocatalytic asymmetric [3+2] cycloaddition of N-2,2,2-trifluoroethyl isatin ketimines with cyclic 2,4-dienones

作者:Chuncheng Zou[1,2];Yuanyuan Han[1];Chuikun Zeng[1];Tony YZhang[1];Jinxing Ye[1];Gonghua Song[2]

机构:[1]Engineering Research Center of Pharmaceutical Process Chemistry,Ministry of Education,East China University of Science and Technology,Shanghai 200237,China;[2]Shanghai Key Laboratory of Chemistry Biology,East China University of Science and Technology,Shanghai 200237,China

年份:2020

卷号:31

期号:2

起止页码:377

中文期刊名:Chinese Chemical Letters

外文期刊名:中国化学快报(英文版)

收录:CSTPCD;;Scopus;CSCD:【CSCD2019_2020】;

基金:supported by the National Natural Science Foundation of China(Nos.21272068,21572056,21801077);China Postdoctoral Science Foundation(Nos.2017M621382,2018T110355);Shanghai Sailing Program(No.18YF1406200);the Fundamental Research Funds for the Central Universities。

语种:英文

中文关键词:Organocatalysis;Spiro;oxindole;skeleton;[3+2]cycloaddition;Cyclic;2,4-dienones;CF3;group

外文关键词:Organocatalysis;Spiro oxindole skeleton;[3+2] cycloaddition;Cyclic 2,4-dienones;CF3 group

摘要:An organocatalytic asymmetric [3+2] cycloaddition of trifluoromethyl-containing azomethine ylides with cyclic 2,4-dienones was developed.The process enables efficient incorporation of CF3 groups into functionalized spiro [pyrro lid in-3,2'-oxindoles] in high yields with good to excellent enantio-and diastereoselectivities.
An organocatalytic asymmetric [3+2] cycloaddition of trifluoromethyl-containing azomethine ylides with cyclic 2,4-dienones was developed.The process enables efficient incorporation of CF3 groups into functionalized spiro [pyrro lid in-3,2’-oxindoles] in high yields with good to excellent enantio-and diastereoselectivities.

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