Mining Sequence Space for Asymmetric Aminocatalysis: N-Terminal Prolyl-Peptides 
Efficiently Catalyze Enantioselective Aldol and Michael Reactions

Martin, Harry J.; List, Benjamin

doi:10.1055/s-2003-41490

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Mining Sequence Space for Asymmetric Aminocatalysis: N-Terminal Prolyl-Peptides Efficiently Catalyze Enantioselective Aldol and Michael Reactions

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Citation

Martin, H. J., & List, B. (2003). Mining Sequence Space for Asymmetric Aminocatalysis: N-Terminal Prolyl-Peptides Efficiently Catalyze Enantioselective Aldol and Michael Reactions. Synlett, 2003(12), 1901-1902. doi:10.1055/s-2003-41490.

Cite as: https://hdl.handle.net/11858/00-001M-0000-0014-A4BE-E

Abstract

N-Terminal prolyl-peptides efficiently catalyze asymmetric aldol and Michael reactions between acetone and p-nitrobenzaldehyde or β-nitrostyrene, respectively.