Enantiospecific and Iterative Suzuki-Miyaura Cross-Couplings

被引:160
作者
Rygus, Jason P. G. [1 ]
Crudden, Cathleen M. [1 ,2 ]
机构
[1] Queens Univ, Dept Chem, Chernoff Hall, Kingston, ON K7L 3N6, Canada
[2] Nagoya Univ, Inst Transformat Biomol WPI ITbM, Chikusa Ku, Nagoya, Aichi 4648601, Japan
基金
加拿大创新基金会; 加拿大自然科学与工程研究理事会;
关键词
CATALYTIC ASYMMETRIC HYDROBORATION; SINGLE-ELECTRON TRANSMETALATION; TERTIARY BORONIC ESTERS; PROTECTING GROUP-FREE; ENANTIOSELECTIVE SYNTHESIS; LITHIATION-BORYLATION; STEREOCHEMICAL COURSE; SECONDARY ALCOHOLS; ARYL; ACID;
D O I
10.1021/jacs.7b08326
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The Suzuki-Miyaura cross-coupling reaction has emerged as one of the most powerful methods for the construction of carbon-carbon bonds. Though most widely utilized for the synthesis of sp(2)-sp(2) linkages, the use of this reaction to form stereochemistry-bearing sp(2)-sp(3) bonds has received widespread attention over the past decade. This Perspective highlights approaches to the synthesis of enantioenriched molecules via the Suzuki-Miyaura reaction. Particular focus is placed on the use of enantiomerically enriched organoboron compounds as coupling partners in stereospecific processes, as well as the development of enantioconvergent and group-selective reactions. In addition, progress in the development of chemoselective, iterative cross-coupling methods will be discussed.
引用
收藏
页码:18124 / 18137
页数:14
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