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Synfacts 2007(11): 1185-1185
DOI: 10.1055/s-2007-991268
DOI: 10.1055/s-2007-991268
Metal-Catalyzed Asymmetric Synthesis and Stereoselective Reactions
© Georg Thieme Verlag Stuttgart · New York
Reduction of Vinyl Phenyl Sulfones with Bisphosphine Monoxide Ligands
J.-N. Desrosiers, A. B. Charette*
Université de Montréal, Canada
Further Information
Publication History
Publication Date:
24 October 2007 (online)

Significance
Quite recently, Carretero and co-workers have reported the asymmetric conjugate reduction of β,β-disubstituted vinyl 2-pyridyl sulfones (Angew. Chem. Int. Ed. 2007, 46, 3329). However, this methodology is unsuitable for the reduction of the corresponding phenyl sulfones. The authors found that a copper-phosphine catalyzed hydrosilylation of vinyl phenyl sulfones gave the corresponding products in excellent yields and ee values. Furthermore, this system shows good tolerance for aromatic as well as cyclic and acyclic alkyl-substituted substrates.