电泳剂
立体专一性
化学
组合化学
计算机科学
有机化学
催化作用
作者
Hui Wang,Changcheng Jing,Adam Noble,Varinder K. Aggarwal
标识
DOI:10.1002/anie.202008096
摘要
The stereospecific 1,2-migration of boronate complexes is one of the most representative reactions in boron chemistry. This process has been used extensively to develop powerful methods for asymmetric synthesis, with applications spanning from pharmaceuticals to natural products. Typically, 1,2-migration of boronate complexes is driven by displacement of an α-leaving group, oxidation of an α-boryl radical, or electrophilic activation of an alkenyl boronate complex. The aim of this article is to summarize the recent advances in the rapidly expanding field of electrophile-induced stereospecific 1,2-migration of groups from boron to sp
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