Ruthenium- and Rhodium-Catalyzed Strain-Driven Cleavage and Reconstruction of the C-C Bond

被引:49
|
作者
Kondo, Teruyuki [1 ]
机构
[1] Kyoto Univ, Adv Biomed Engn Res Unit, Ctr Promot Interdisciplinary Educ & Res, Nishikyo Ku, Kyoto 6158510, Japan
基金
日本科学技术振兴机构;
关键词
Strained molecules; Cleavage reactions; Homogenous catalysis; Ruthenium; Rhodium; CARBON-CARBON BOND; ADDITION/RING-OPENING REACTION; TERT-CYCLOBUTANOLS; RING EXPANSION; STEREOSPECIFIC DIMERIZATION; BINOR-S; TRICARBONYL(VINYLKETENE)IRON(0) COMPLEXES; ENANTIOSELECTIVE SYNTHESIS; REGIOSELECTIVE-SYNTHESIS; LINEAR CODIMERIZATION;
D O I
10.1002/ejoc.201501291
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The synthesis of new functional organic molecules that cannot be obtained by a simple combination of conventional synthetic methods is a challenging subject in organic, organometallic, and industrial chemistry as well as in atom-efficient and environmental organic synthesis. Among the various possibilities that have been considered, the catalytic cleavage and reconstruction of the C-C bond has opened the door to a new branch of synthetic organic chemistry. This microreview summarizes progress on the ruthenium-and rhodium-catalyzed strain-driven cleavage of the C-C bond, the methods of which were mostly developed by the author. The direct oxidative addition of 2,5-norbornadienes, cyclopropenones, cyclobutenones, and cyclobutenediones, and to catalytically active metal species followed by the construction of the C-C bond has been used for the preparation of new organic molecules.
引用
收藏
页码:1232 / 1242
页数:11
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