Metal-catalyzed activation of ethers via C-O bond cleavage: a new strategy for molecular diversity

被引:596
作者
Cornella, Josep [1 ]
Zarate, Cayetana [1 ]
Martin, Ruben [1 ,2 ]
机构
[1] Inst Chem Res Catalonia ICIQ, Tarragona 43007, Spain
[2] Catalan Inst Res & Adv Studies ICREA, Barcelona 08010, Spain
基金
欧洲研究理事会;
关键词
CROSS-COUPLING REACTIONS; CARBON-OXYGEN BONDS; N-HETEROCYCLIC CARBENES; ARYL GRIGNARD-REAGENTS; REDUCTIVE CLEAVAGE; METHYL ETHERS; ORGANOBORON COMPOUNDS; OXIDATIVE ADDITION; PHENOL DERIVATIVES; ORGANIC-SYNTHESIS;
D O I
10.1039/c4cs00206g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In 1979, the seminal work of Wenkert set the standards for the utilization of aryl and vinyl ethers as coupling partners via C-O bond-cleavage. Although the topic remained dormant for almost three decades, the last few years have witnessed a renaissance in this area of expertise, experiencing an exponential growth and becoming a significant discipline within the cross-coupling arena. The means to utilize readily accessible aryl or vinyl ethers as counterparts does not only represent a practical, powerful and straightforward alternative to organic halides, but also constitutes an excellent opportunity to improve our chemical knowledge about a relatively unexplored area of expertise. This review summarizes the most significant developments in the area of C-O bond-cleavage when employing aryl or vinyl ethers, providing a detailed overview of the current state of the art and including future aspects, when applicable.
引用
收藏
页码:8081 / 8097
页数:17
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