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镍催化烯基硼酸酯的高选择性氢烯丙基化反应以获得烯丙基硼酸。

Nickel-Catalyzed Highly Selective Hydroalkenylation of Alkenyl Boronic Esters to Access Allyl Boron.

机构信息

Institute of Molecular Plus, Tianjin Key Laboratory of Molecular Optoelectronic Science, Department of Chemistry, School of Science, Tianjin University, Weijin Road 92, Tianjin 300072, China.

出版信息

Org Lett. 2020 Nov 6;22(21):8285-8290. doi: 10.1021/acs.orglett.0c02923. Epub 2020 Oct 22.

Abstract

Allyl boron derivatives are valuable building blocks in the synthesis of natural products and bioactive molecules. Herein, a practical strategy of nickel-catalyzed highly selective hydroalkenylation of alkenyl boronic esters was developed. Under the mild reaction conditions, a variety of allyl boronic esters were accessed with excellent chemo- and regioselectivity. The mechanism of this transformation was illustrated by control experiments and kinetic studies.

摘要

烯丙基硼酸衍生物是合成天然产物和生物活性分子的重要构建模块。本文开发了一种镍催化的烯基硼酸酯高选择性氢烯丙基化的实用策略。在温和的反应条件下,各种烯丙基硼酸酯以优异的化学和区域选择性得到了很好的合成。通过对照实验和动力学研究说明了这种转化的机制。

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