Metal-Catalyzed Carbon-Carbon Bond Cleavage of Unstrained Alcohols

被引:158
作者
Lutz, Marius D. R. [1 ]
Morandi, Bill [1 ]
机构
[1] Swiss Fed Inst Technol, CH-8093 Zurich, Switzerland
基金
欧洲研究理事会;
关键词
C-H BOND; ASYMMETRIC CONJUGATE ALKYNYLATION; O-BROMOBENZYL ALCOHOLS; BETA-HYDRIDE ELIMINATION; INTERNAL ALKYNES; CARBONYLATIVE ANNULATION; LIGNIN DEPOLYMERIZATION; PROPARGYL ALCOHOLS; ALPHA-ARYLATION; ARYL BROMIDES;
D O I
10.1021/acs.chemrev.0c00154
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The functionalization of molecules by cleaving inert carbon-carbon single bonds is regarded as a great synthetic challenge due to their inherent stability. In recent years, significant progress has been made in the activation of small rings relying on the release of strain energy. By contrast, the number of catalytic methodologies for the activation of unstrained carbon-carbon single bonds is still limited. This review focuses on the recent developments in transition-metal-catalyzed cleavage of C-C bonds in unstrained alcohols via beta-carbon elimination. Emphasis is placed on the mechanistic aspects of the discussed transformations and their applications to the deconstruction and reorganization of molecules.
引用
收藏
页码:300 / 326
页数:27
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