Kwon Su Jin, Kim Dae Young
Department of Chemistry, Soonchunhyang University, Asan, Chungnam 31538.
Chem Rec. 2016 Jun;16(3):1191-203. doi: 10.1002/tcr.201600003. Epub 2016 Apr 7.
The direct functionalization of C(sp(3) )-H bonds is one of the most synthetically powerful research areas in current organic synthesis. Organocatalytic C(sp(3) )-H bond activation reactions have recently been developed in addition to the traditional metal-catalyzed C(sp(3) )-H activation reactions. In this review, we aim to give a brief overview of organo- and organometallic internal redox cascade reactions with respect to the mechanism, the reactivity of hydrogen donors and acceptors, and the migration modes of hydrogen.
C(sp(3) )-H键的直接官能团化是当前有机合成中最具合成潜力的研究领域之一。除了传统的金属催化C(sp(3) )-H活化反应外,有机催化C(sp(3) )-H键活化反应近年来也得到了发展。在本综述中,我们旨在从机理、氢供体和受体的反应性以及氢的迁移模式等方面,对有机和有机金属内部氧化还原级联反应作简要概述。