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作 者:Wujun Jian Mong-Feng Chiou Yajun Li Hongli Bao Song Yang
机构地区:[1]National Key Laboratory of Green Pesticide,Key Laboratory of Green Pesticide and Agricultural Bioengineering,Ministry of Education,Center for R&D of Fine Chemicals of Guizhou University,Guiyang 550025,China [2]Strait Institute of Flexible Electronics(SIFE,Future Technologies),Fujian Normal University,Fuzhou 350117,China [3]Key Laboratory of Coal to Ethylene Glycol and Its Related Technology,State Key Laboratory of Structural Chemistry,Fujian Institute of Research on the Structure of Matter,University of Chinese Academy of Sciences,Fuzhou 350002,China
出 处:《Chinese Chemical Letters》2024年第5期141-144,共4页中国化学快报(英文版)
基 金:supported by the National Natural Science Foundation of China(NSFC,Nos.22001251,21922112,and 22225107);the Strategic Priority Research Program of the Chinese Academy of Sciences(No.XDB20000000);National Key R&D Program of China(No.2017YFA0700103);the Guizhou Provincial S&T Project(No.2018[4007]).
摘 要:Borylation of 1,3-enynes with bis(boronate)compounds often ends up with the formation of hydroborylated products,leaving the diborylation of 1,3-enynes for the formation of 1,4-diborylated allenes to be challenging.Herein,a copper-catalyzed chemo-,regio-,and stereo-selective diborylation of 1,3-enynes for the efficient construction of 1,4-diborylated allenes under base-free conditions was reported.A wide range of 1,3-enynes bearing various functional groups can participant in the reaction and afforded the corresponding 1,4-diborylated allenes in good to excellent yields,which was enabled by the protocol of Bpin to BF3K conversion.the borylcopper species was supposed to selectively attack the C-C triple bond of the 1,3-enynes.
关 键 词:Copper catalysis REGIOSELECTIVE 1 3-Enynes BORYLATION ALLENES
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