Decarboxylative Borylation: New Avenues for the Preparation of Organoboron Compounds

Decarboxylative Borylation: New Avenues for the Preparation of Organoboron Compounds
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脱羧硼化:制备有机硼化合物的新途径

DOI:
10.1002/ejoc.201800534
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发表时间:
2018-06
影响因子:
2.8
通讯作者:
Xu Liang
Xu Liang
中科院分区:
化学3区
文献类型:
--
作者:
Xu Liang

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有机硼化合物的制备在有机化学中得到了广泛的探索和不懈的追求。最近,氧化还原活化的N-羟基邻苯二甲酰亚胺羧酸酯已被用作脱羧硼化过程的有效原料,使丰富的羧酸和通用的有机硼化合物之间的偶联成为可能。在这里,我们强调这些进展,重点是澄清镍催化,光促进或有机催化脱羧硼化反应的不同工作机制。
The preparation of organoboron compounds has been widely explored and persistently pursued in organic chemistry. Recently, redox‐activatedN‐hydroxyphthalimide carboxylic esters have been utilized as efficient feedstocks for decarboxylative borylation processes, enabling coupling between the abundant carboxylic acids and the versatile organoboron compounds. Here we highlight such advances, with an emphasis on clarifying the different working mechanisms for Ni‐catalyzed, light‐promoted, or organocatalytic decarboxylative borylative reactions.
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