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Issue 8, 2010
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Chemoselective olefinmetathesis transformations mediated by ruthenium complexes

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Abstract

Over the past decade, ruthenium-mediated metathesis transformations, including polymerization reactions, cross-metathesis, ring-closing metathesis, enyne metathesis, ring-rearrangement metathesis, and also tandem processes, represent one of the most studied families of organic reactions. This has translated into the development of a large number of structurally diverse catalysts. Whereas most of these investigations are focused on determining catalytic performance, only rare examples of studies dealing with chemoselectivity have been reported to date. Usually, variations are observed in product conversions but rarely in product distributions. In this critical review, we provide an overview of the stereochemistry of newly formed C[double bond, length as m-dash]C bonds either in ring-closing or cross-metathesis as a function of the catalyst structure. A discussion of disparities encountered in macrocyclisation reactions leading (or not) to the formation of dimeric products is also presented. Since distinctive metathesis products could be isolated as a function of the ligand borne by the ruthenium centre—phosphine or N-heterocyclic carbene in the dissymetrization of trienes, enyne metathesis and ring rearrangements, these topics are also discussed (72 references).

Graphical abstract: Chemoselective olefin metathesis transformations mediated by ruthenium complexes

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Publication details

The article was received on 19 Feb 2010 and first published on 30 Jun 2010


Article type: Critical Review
DOI: 10.1039/B912410C
Chem. Soc. Rev., 2010,39, 3305-3316

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    Chemoselective olefin metathesis transformations mediated by ruthenium complexes

    S. P. Nolan and H. Clavier, Chem. Soc. Rev., 2010, 39, 3305
    DOI: 10.1039/B912410C

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