Stereoselective synthesis of chiral α-amino-β-lactams through palladium(II)-catalyzed sequential monoarylation/amidation of C(sp 3)-H Bonds

Angewandte Chemie - International Edition

Volumn 52, Issue 51, 2013, Pages 13588-13592

  Zhang, Qi ^a   Chen, Kai ^a   Rao, Weihao ^a   Zhang, Yuejun ^a,b   Chen, Fa Jie ^a   Shi, Bing Feng ^a  

^a ZHEJIANG UNIVERSITY   (China)

^b SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY   (China)

Author keywords

lactams; amidation; arylation; C H activation; palladium

Indexed keywords

AMIDATION; ARYL SUBSTITUENTS; ARYLATIONS; C-H ACTIVATION; DIASTEREO-SELECTIVITY; MONOARYLATION; PALLADIUM CATALYSIS; STEREOSELECTIVE SYNTHESIS;

ACTIVATION ANALYSIS; AMINO ACIDS; AROMATIC COMPOUNDS; CATALYSIS; FUNCTIONAL GROUPS; PALLADIUM; PALLADIUM COMPOUNDS; STEREOCHEMISTRY; STEREOSELECTIVITY; SUBSTITUTION REACTIONS;

AMIDES;

BETA LACTAM; PALLADIUM;

AMIDATION; ARTICLE; ARYLATION; C H ACTIVATION; CATALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; STEREOISOMERISM; SYNTHESIS; Β-LACTAMS;

AMIDATION; ARYLATION; C H ACTIVATION; PALLADIUM; Β-LACTAMS;

BETA-LACTAMS; CATALYSIS; MOLECULAR STRUCTURE; PALLADIUM; STEREOISOMERISM;

EID: 84890477776     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201306625     Document Type: Article

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