Rhodium-catalyzed, highly enantioselective 1,2-addition of aryl boronic acids to α-ketoesters and α-diketones using simple, chiral sulfur-olefin ligands

Angewandte Chemie - International Edition

Volumn 51, Issue 3, 2012, Pages 780-783

  Zhu, Ting Shun ^a   Jin, Shen Shuang ^a   Xu, Ming Hua ^a  

^a SHANGHAI INSTITUTE OF MATERIA MEDICA   (China)

Author keywords

hydroxy carbonyl compounds; 1,2 addition; asymmetric catalysis; rhodium; sulfur olefin ligands

Indexed keywords

1,2-ADDITION; ASYMMETRIC CATALYSIS; BORONIC ACID; DIKETONES; ENANTIOSELECTIVE; HYDROXY CARBONYLS; KETO ESTER; RHODIUM CATALYSIS; RHODIUM-CATALYZED; ROOM TEMPERATURE;

CATALYSIS; ENANTIOSELECTIVITY; KETONES; OLEFINS; RHODIUM; SULFUR;

LIGANDS;

ALKENE; BORONIC ACID DERIVATIVE; KETONE; LIGAND; RHODIUM; SULFUR;

ARTICLE; CATALYSIS; CHEMISTRY; STEREOISOMERISM;

ALKENES; BORONIC ACIDS; CATALYSIS; KETONES; LIGANDS; RHODIUM; STEREOISOMERISM; SULFUR;

EID: 84855793878     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201106972     Document Type: Article

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