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Halo-substituted benzenesulfonyls and benzenesulfinates: Convenient sources of arenes in metal-catalyzed C-C bond formation reactions for the straightforward access to halo-substituted arenes

Abstract

Palladium-catalyzed reactions using aryl halides as one of the coupling partners represent a very popular method for generating carbon–carbon bonds. However, such couplings suffer of important limitations. As most palladium catalysts are very effective for the cleavage of C-halo bonds (Halo = Cl, Br or I), in many cases, the presence of several halide functional groups on arenes is not tolerated. Since two decades, and especially during the last few years, a new class of coupling partners: benzenesulfonyl and benzenesulfinate derivatives has emerged as a powerful alternative to aryl halides for the Pd-catalyzed C-C bond formation, as the reactions performed with these substrates generally tolerate C-halo bonds. With these substrates, after a metal-catalyzed desulfitative coupling, a variety of halo-substituted arenes such as biaryls, styrenes, phenylacetylenes, acetophenones, benzonitriles… has been synthetized with high chemoselectivities. The use of these aryl sources allowed the synthesis of molecules containing several halo-substituents including iodo-substituents in only a few steps, and provides a very simple access to a very wide variety of halo-substituted arenes useful to material chemists and also to biochemists. In this review, we will summarize the scope of the use of halo-substituted benzenesulfonyls and benzenesulfinates as coupling partners in metal-catalyzed C-C bond formation.

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Publication details

The article was received on 14 Mar 2018, accepted on 09 May 2018 and first published on 09 May 2018


Article type: Review Article
DOI: 10.1039/C8OB00632F
Citation: Org. Biomol. Chem., 2018, Accepted Manuscript
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    Halo-substituted benzenesulfonyls and benzenesulfinates: Convenient sources of arenes in metal-catalyzed C-C bond formation reactions for the straightforward access to halo-substituted arenes

    H. Li, A. Sasmal, X. Shi, J. Soule and H. Doucet, Org. Biomol. Chem., 2018, Accepted Manuscript , DOI: 10.1039/C8OB00632F

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