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Synfacts 2008(10): 1078-1078
DOI: 10.1055/s-2008-1078236
DOI: 10.1055/s-2008-1078236
Metal-Catalyzed Asymmetric Synthesis and Stereoselective Reactions
© Georg Thieme Verlag
Stuttgart ˙ New York
Diastereoselective Addition of Allylzinc Reagents to Sulfinimines
L. R. Reddy*, B. Hu, M. Prashad, K. Prasad
Novartis Pharmaceuticals Corporation, East Hanover, USA
Further Information
Publication History
Publication Date:
22 September 2008 (online)
Significance
The diastereoselective addition of organometallic reagents to chiral sulfinimines is a well-known method for generating new stereocenters, and examples of addition of unsubstituted allylmagnesium reagents are abundant. In this work the authors report the efficient asymmetric addition of substituted racemic allylzinc reagents to Ellman’s imine (1). Formation of homoallylic amines bearing two new stereocenters in excellent yield and diastereoselectivity is described.