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Synfacts 2006(10): 1039-1039
DOI: 10.1055/s-2006-949320
DOI: 10.1055/s-2006-949320
Metal-Catalyzed Asymmetric Synthesis and Stereoselective Reactions
© Georg Thieme Verlag Stuttgart · New York
Conjugate Addition and Subsequent Enolate Trapping with Electrophiles
X. Rathgeb, S. March, A. Alexakis*
University of Geneva, Switzerland
Further Information
Publication History
Publication Date:
21 September 2006 (online)
Significance
Asymmetric conjugate addition is one of the most powerful methods for C-C bond formation at the β-carbon. The potential exists for further elaboration at the α-carbon by in situ trapping of the metal enolate with electrophiles. The authors describe trapping of poorly reactive zinc enolates with activated electrophiles giving good to high yields and trans/cis products with excellent enantioselectivity.