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        劉永宏研究團隊在《ANGEWANDTE CHEMIE-INTERNATIONAL EDITION》發(fā)表論文

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        時(shí)間:2018-06-04  作者:LMB  來(lái)源:文本大小:【 |  | 】  【打印

        題目: Bifunctional Ligand Enables Efficient Gold-Catalyzed Hydroalkenylation of Propargylic Alcohol

        作者: Shengrong Liao, Alessio Porta, Xinpeng Cheng, XuMa, Giuseppe Zanoni,* and Liming Zhang*

        刊物: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

        年卷期頁(yè): 2018, 57, 8250-8254

        摘要:Using the previously designed biphenyl-2-ylphosphine ligand, featuring a remote tertiary amino group, the first gold-catalyzed intermolecular hydroalkenylation of alkynes has been developed. Synthetically valuable conjugated dienyl alcohols are formed in moderate to good yields. A range of alkenyltrifluoroborates are allowed as the alkenyl donor, and no erosion of alkene geometry and/or the propargylic configuration are detected. DFT calculations confirm the critical role of the remote basic group in the ligand as a general-base catalyst for promoting this novel gold catalysis with good efficiency.

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