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Asymmetric intramolecular oxa-Michael reactions to tetrahydrofurans/2H- pyrans catalyzed by primary-secondary diamines  ( EI收录)  

文献类型:期刊文献

英文题名:Asymmetric intramolecular oxa-Michael reactions to tetrahydrofurans/2H- pyrans catalyzed by primary-secondary diamines

作者:Lu, Yingpeng[1,2]; Zou, Gang[1]; Zhao, Gang[2]

机构:[1] Laboratory of Advanced Materials, Institute of Fine Chemicals, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, China; [2] Key Laboratory of Synthetic Chemistry of Natural Substances, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, China

年份:2013

卷号:3

期号:6

起止页码:1356

外文期刊名:ACS Catalysis

收录:EI(收录号:20132616447766)

语种:英文

外文关键词:Catalysis - Ketones - Addition reactions

摘要:The asymmetric intramolecular oxa-Michael reactions of α,β- unsaturated ketones have been achieved by using readily accessible primary-secondary diamines as the organocatalysts, giving the synthetically useful tetrahydrofurans/2H-pyrans in good yields and with high enantioselectivities (up to 90% ee). ? 2013 American Chemical Society.

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