Pd(II)-catalyzed regio-, enantio-, and diastereoselective 1,4-addition of azlactones formed in situ from racemic unprotected amino acids and acetic anhydride

Journal of Organic Chemistry

Volumn 77, Issue 23, 2012, Pages 10846-10855

  Weber, Manuel ^a   Peters, René ^a  

^a UNIVERSITY OF STUTTGART   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

1 ,4-ADDITION; ACETIC ANHYDRIDES; AMINO ACID DERIVATIVES; AZLACTONES; BENZOIC ANHYDRIDE; DIASTEREOSELECTIVE; ENANTIO; MULTI-COMPONENT REACTIONS; PRODUCT MIXTURE;

AMINO ACIDS; CATALYSTS; REACTION KINETICS;

PALLADIUM COMPOUNDS;

ACETIC ANHYDRIDE; ALANINE; ALPHA AMINO ACID; AMINO ACID; AZLACTONE DERIVATIVE; LACTONE; PALLADIUM; PENTAPHENYLFERROCENE MONOPALLADACYCLE; UNCLASSIFIED DRUG;

ADDITION REACTION; ARTICLE; CATALYSIS; CATALYST; ENANTIOSELECTIVITY; HYDROLYSIS; MICHAEL ADDITION; RACEMIC MIXTURE;

ACETIC ANHYDRIDES; AMINO ACIDS; CATALYSIS; LACTONES; MOLECULAR STRUCTURE; PALLADIUM; STEREOISOMERISM;

EID: 84870931097     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo302177t     Document Type: Article

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