硼酸化
化学
背景(考古学)
区域选择性
催化作用
铱
范围(计算机科学)
组合化学
有机化学
计算机科学
芳基
古生物学
烷基
生物
程序设计语言
作者
Liang Xu,Guanghui Wang,Shuai Zhang,Hong Wang,Linghua Wang,Li Liu,Jiao Jiao,Pengfei Li
出处
期刊:Tetrahedron
[Elsevier BV]
日期:2017-11-06
卷期号:73 (51): 7123-7157
被引量:275
标识
DOI:10.1016/j.tet.2017.11.005
摘要
In the past decades, the iridium-catalyzed C–H bond borylation and other newly discovered catalytic borylation reactions have received extensive research interests and developed into a practical approach for functionalization of C−H bonds and therefore an effective and versatile tool in synthesis of novel organic materials, natural products and fine chemicals. The advances of this booming field include significant improvements of the venerable iridium-catalyzed borylation and development of other transition-metal, especially the first-row transition-metal catalyzed borylation. More recently, a metal-free catalytic borylation system has been disclosed. These new methodologies has dramatically expanded the substate scope, increased the reaction efficiency, lowered the cost, and more importantly, provided previously unknown complementary chemical and regioselectivity. During these discoveries, novel catalyst design concepts and/or principles have been generated. In this context, this review aims to detail the recent evolution in the exciting research direction, focusing on the discovery and development of new reactivity, new selectivity.
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