立体中心
镍
催化作用
环加成
试剂
还原消去
反应中间体
组合化学
化学
有机合成
计算化学
功能群
过渡金属
戒指(化学)
有机化学
对映选择合成
聚合物
标识
DOI:10.1002/anie.200300634
摘要
Abstract For over 50 years, nickel catalysis has been applied in cycloaddition processes. Nickel‐catalyzed reductive couplings and cyclizations, however, have only recently attracted a high level of interest. This group of new reactions allows a broad range of multicomponent couplings involving two or more π components with a main‐group or transition‐metal reagent. These processes allow the assembly of important organic substructures from widely available reaction components. Multiple contiguous stereocenters, polycyclic ring systems, and novel arrays of complex functionality may often be prepared from simple, achiral, acyclic precursors. With three or more reactive functional groups participating in the catalytic processes, many mechanistic questions abound, including the precise timing of bond constructions and the nature of reactive intermediates. This Review is thus aimed at providing a critical evaluation of recent progress in this rapidly developing field.
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