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Synlett 2003(12): 1901-1902
DOI: 10.1055/s-2003-41490
DOI: 10.1055/s-2003-41490
CLUSTER
© Georg Thieme Verlag Stuttgart · New YorkMining Sequence Space for Asymmetric Aminocatalysis: N-Terminal Prolyl-Peptides Efficiently Catalyze Enantioselective Aldol and Michael Reactions
Further Information
Received
28 February 2003
Publication Date:
19 September 2003 (online)
Publication History
Publication Date:
19 September 2003 (online)

Abstract
N-Terminal prolyl-peptides efficiently catalyze asymmetric aldol and Michael reactions between acetone and p-nitrobenzaldehyde or β-nitrostyrene, respectively.
Key words
organocatalysis - enamine catalysis - aminocatalysis - peptides
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References
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