Potential of Metal-Catalyzed C–C Single Bond Cleavage for Organic Synthesis

Conventional organic synthesis has been mainly based upon the reactivities of π-bonds and polar σ-bonds. Carbon–carbon single bonds are nonpolar and generally far less reactive. Although they remain intact under most reaction conditions, it is possible to activate and cleave them if suitable organom...

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Veröffentlicht in:Journal of the American Chemical Society 2016-10, Vol.138 (42), p.13759-13769
Hauptverfasser: Murakami, Masahiro, Ishida, Naoki
Format: Artikel
Sprache:eng
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Zusammenfassung:Conventional organic synthesis has been mainly based upon the reactivities of π-bonds and polar σ-bonds. Carbon–carbon single bonds are nonpolar and generally far less reactive. Although they remain intact under most reaction conditions, it is possible to activate and cleave them if suitable organometallic compounds or metal catalysts are applied. Such C–C single bond cleavage reactions are attracting increasing attention in the context of synthetic chemistry because they provide a unique and more straightforward route from readily available substances to targets, while requiring significantly fewer steps. The present Perspective aims to exemplify the potential of metal-catalyzed C–C single bond cleavage for organic synthesis.
ISSN:0002-7863
1520-5126
DOI:10.1021/jacs.6b01656