Recent advances in transition-metal-catalyzed functionalization of unstrained carbon-carbon bonds

Feng Chen, Teng Wang, Ning Jiao

Research output: Contribution to journalReview articlepeer-review

756 Scopus citations

Abstract

Some recent advances in transition-metal complex catalyzed cleavage of unstrained carbon-carbon bonds, including C-C single bonds, C-C double bonds, and C-C triple bonds was reported. Many examples of unstrained C-C single bond cleavage catalyzed by various transition-metal complexes have been reported. Generally, functional groups adjacent to these bonds are necessary for these transformations. In the developed methods, oxidative addition, βcarbon elimination, decarbonylation, and retroallyation are common mechanisms for transition-metal complex catalyzed C-C single bond functionalization. Olefin metathesis and enyne metathesis reactions are very important methods for C=C double bond cleavage, and they have been well developed. Additionally, oxidative cleavage is another class of C=C bond activation process. Many transition-metal complexes have been developed for this kind of reaction using appropriate oxidants, especially molecular oxygen. Various mechanisms are proposed for cleavage of carbon-carbon bonds. The further development of new carbon-carbon bond cleavage reactions in this field will be expected to explore new catalytic systems with inexpensive transition-metal catalysts, under mild conditions, with green and sustainable oxidants, and with a wide substrate scope.

Original languageEnglish (US)
Pages (from-to)8613-8661
Number of pages49
JournalChemical Reviews
Volume114
Issue number17
DOIs
StatePublished - Sep 10 2014

Bibliographical note

Funding Information:
Financial support from the National Natural Science Foundation of China (Grants 21325206 and 21172006), National Young Top-notch Talent Support Program, and Ph.D. Programs Foundation of the Ministry of Education of China (Grant 20120001110013) is greatly appreciated.

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