文献类型：期刊文献

中文题名：Fc-PIP Catalyzed Asymmetric Synthesis of cis-2,3-Dihydrobenzofurans

作者：Shanshan Jiang[1];Bin Hu[1];Xingxin Yu[1];Weiping Deng[1]

机构：[1]Shanghai Key Laboratory of New Drug Design,School of Pharmacy,East China University of Science and Technology,Shanghai 200237,China

年份：2014

卷号：32

期号：8

起止页码：694

中文期刊名：Chinese Journal of Chemistry

外文期刊名：中国化学（英文版）

收录：CSTPCD;;Scopus;CSCD:【CSCD2013_2014】；PubMed;

基金：The authors are grateful to the Fundamental Research Funds for the Central Universities,the National Natural Science Foundation of China(No.21372074).

语种：英文

中文关键词：Michael addition-Lactonization;dihydrobenzofuran;Fc-PIP

摘要：A highly enantioselective intramolecular Michael addition-Lactonization domino reaction of a range of enon acids catalyzed by nuleophilic organocatalyst(Fc-PIP)was developed,furnishing cis-2,3-dihydrobenzofuran derivatives with excellent enantioselecitivities(94%-98%ee)and good diastereoselectivities(up to 99/1).