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作 者:Bao-xin Liu Ru-Jie Yan Wei Du Ying-Chun Chen
机构地区:[1]Key Laboratory of Drug-Targeting and Drug Delivery System of the Education Ministry and Sichuan Province,and Sichuan Research Center for Drug Precision Industrial Technology,West China School of Pharmacy,Sichuan University,Chengdu,Sichuan 610041,China [2]College of Pharmacy,Third Military Medical University,Shapingba,Chongqing 400038,China
出 处:《Chinese Journal of Chemistry》2022年第10期1185-1189,共5页中国化学(英文版)
基 金:We are grateful for the financial support from the NSFC(Nos.21931006 and 21921002);the Fundamental Research Funds for the Central Universities.
摘 要:A solvent-regulated diastereodivergent[3+2]annulation reaction between Morita-Baylis-Hillman carbonates from aryl trifluoromethyl ketones and cyclic sulfonimines is developed under the catalysis of a modified cinchona alkaloid,furnishing diverse polycyclic products bearing vicinal quaternary stereogenic centers with outstanding enantioselectivity and moderate to high diastereoselectivity.
关 键 词:Diastereodivergent synthesis [3+2]annulation Trifluoromethyl group Lewis bases Solvent effects
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