Synlett 2021(12): 1901-1902  
DOI: 10.1055/s-2003-41490
CLUSTER
© Georg Thieme Verlag Stuttgart · New York

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

Harry J. Martin, Benjamin List*
Department of Molecular Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, USA
Fax: +1(858)7847028; e-Mail: blist@scripps.edu.;
Further Information

Publication History

Received 28 February 2003
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.

1

New Address: Max-Plank-Institut für Kohlenforschung, 45470 Mülheim an der Ruhr, Germany.
E-mail: list@mpi-muelheim-mpg.de