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

Synlett

Volumn , Issue 12, 2003, Pages 1901-1902

  Martin, Harry J ^a   List, Benjamin ^a,b  

^a SCRIPPS RESEARCH INSTITUTE   (United States)

^b MAX PLANCK INSTITUT FÜR KOHLENFORSCHUNG   (Germany)

Author keywords

Aminocatalysis; Enamine catalysis; Organocatalysis; Peptides

Indexed keywords

4 NITROBENZALDEHYDE; ACETONE; BENZALDEHYDE DERIVATIVE; NITROSTYRENE; PEPTIDE DERIVATIVE; PROLYLALANINE; PROLYLARGININE; PROLYLASPARTIC ACID; PROLYLGLUTAMIC ACID; PROLYLGLYCYLGLYCINE; PROLYLHISTIDYLALANINE; PROLYLHYDROXIDE; PROLYLLYSINE; PROLYLSERINE; PROLYLTRYPTOPHAN; PROLYLVALINE; STYRENE DERIVATIVE; UNCLASSIFIED DRUG;

ALDOL REACTION; AMINO TERMINAL SEQUENCE; ARTICLE; ASYMMETRIC CATALYSIS; ENANTIOSELECTIVITY; MICHAEL ADDITION; REACTION ANALYSIS; SEQUENCE ANALYSIS;

EID: 0142091323     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2003-41490     Document Type: Article

References (33)

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