Qi Xinxin, Jiang Li-Bing, Zhou Chao, Peng Jin-Bao, Wu Xiao-Feng
Department of Chemistry Zhejiang Sci-Tech University Xiasha Campus Hangzhou 310018 P.R. China.
Leibniz-Institut für Katalyse e.V. an der Universität Rostock Albert-Einstein-Straße 29a 18059 Rostock Germany.
ChemistryOpen. 2017 Mar 16;6(3):345-349. doi: 10.1002/open.201700036. eCollection 2017 Jun.
A convenient and general zinc-catalyzed borylation of aryl diazonium salts and aryltriazenes has been developed. With bis- (pinacolato)diboron as the borylation reagent, aryldiazonium tetrafluoroborate salts and aryltriazenes were transformed into the corresponding arylboronates in moderate to excellent yields under mild conditions. As a convenient and practical methodology, no additional ligands, base, or any other additives are required here.
已开发出一种便捷通用的锌催化芳基重氮盐和芳基三氮烯的硼化反应。以双(频哪醇合)二硼作为硼化试剂,在温和条件下,四氟硼酸芳基重氮盐和芳基三氮烯被转化为相应的硼酸芳基酯,产率适中至优异。作为一种便捷实用的方法,此反应无需额外的配体、碱或任何其他添加剂。