Wen Yanmei, Xie Jianying, Deng Chunmei, Li Chaode
†College of Science, Guangdong Ocean University, Zhanjiang 524088, China.
‡State Key Laboratory of Luminescent Materials and Devices, South China University of Technology, Guangzhou 510640, China.
J Org Chem. 2015 Apr 17;80(8):4142-7. doi: 10.1021/jo502606x. Epub 2015 Mar 27.
An efficient copper-catalyzed borylation reaction of allyl or vinyl arenes with bis(pinacolato)diboron has been developed, without using ligands. Markovnikov-selectivity is observed in the borylation of allyl arenes with bis(pinacolato)diboron, while the regioselectivity is completely opposite when styrene derivatives are used as substrates. A mechanism involving Cu-B species regioselectively adding olefin double bonds to form the alkylcopper or η(3)-benzyl copper intermediate, which is followed by protonation to obtain products, is proposed.
已经开发出一种高效的铜催化烯丙基芳烃或乙烯基芳烃与双(频哪醇)二硼的硼化反应,无需使用配体。在用双(频哪醇)二硼对烯丙基芳烃进行硼化反应时观察到马氏选择性,而当使用苯乙烯衍生物作为底物时,区域选择性则完全相反。提出了一种机理,即铜硼物种区域选择性地加成烯烃双键以形成烷基铜或η(3)-苄基铜中间体,随后进行质子化以获得产物。