Bispalladacycle-catalyzed Michael addition of in situ formed azlactones to enones

Chemistry - A European Journal

Volumn 18, Issue 46, 2012, Pages 14792-14804

  Weber, Manuel ^a   Jautze, Sascha ^a   Frey, Wolfgang ^a   Peters, René ^a  

^a UNIVERSITY OF STUTTGART   (Germany)

Author keywords

catalysis; domino processes; dynamic kinetic resolution; peptides; quaternary amino acids

Indexed keywords

ACID PRODUCTS; AMINO ACID DERIVATIVES; ASYMMETRIC ADDITION; ASYMMETRIC CONJUGATE ADDITION; AZLACTONES; BICYCLIC DIPEPTIDES; BULK CHEMICALS; DOMINO PROCESS; DYNAMIC KINETIC RESOLUTION; MICHAEL ADDITIONS; PYROGLUTAMIC ACIDS; STEREOCENTERS; THIRD GENERATION;

ADDITION REACTIONS; CATALYSIS; PEPTIDES;

AMINO ACIDS;

AMINO ACID; PALLADIUM; PROLINE; PYROGLUTAMIC ACID;

ARTICLE; CATALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; STEREOISOMERISM; SYNTHESIS;

AMINO ACIDS; CATALYSIS; MOLECULAR STRUCTURE; PALLADIUM; PROLINE; PYRROLIDONECARBOXYLIC ACID; STEREOISOMERISM;

EID: 84868705068     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201202455     Document Type: Article

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