Montgomery John
Department of Chemistry, Wayne State University, Detroit, MI 48 202-3489, USA.
Angew Chem Int Ed Engl. 2004 Jul 26;43(30):3890-908. doi: 10.1002/anie.200300634.
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 pi 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.
五十多年来,镍催化已应用于环加成反应过程。然而,镍催化的还原偶联和环化反应直到最近才引起高度关注。这组新反应允许涉及两个或更多π组分与主族或过渡金属试剂的广泛多组分偶联。这些过程允许从广泛可得的反应组分组装重要的有机亚结构。多个相邻的立体中心、多环系统和新型复杂官能团阵列通常可以由简单的非手性、无环前体制备。由于有三个或更多反应性官能团参与催化过程,许多机理问题层出不穷,包括键构建的精确时机和反应中间体的性质。因此,本综述旨在对这一快速发展领域的最新进展进行批判性评估。