Inversion or retention? Effects of acidic additives on the stereochemical course in enantiospecific suzuki-miyaura coupling of α-(acetylamino) benzylboronic esters

Journal of the American Chemical Society

Volumn 133, Issue 51, 2011, Pages 20738-20741

  Awano, Tomotsugu ^a   Ohmura, Toshimichi ^a   Suginome, Michinori ^a  

^a KYOTO UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ACIDIC ADDITIVES; ARYL BROMIDES; C-C BOND FORMATION; CATALYST SYSTEM; ENANTIOSPECIFIC; ENANTIOSPECIFICITY; STEREOSPECIFIC; SUZUKI-MIYAURA COUPLING;

BROMINE COMPOUNDS; ESTERIFICATION; ESTERS; PHENOLS; ZIRCONIUM;

ADDITIVES;

ACID; ALPHA(ACYLAMINO)BENZYLBORONIC ESTER; ESTER DERIVATIVE; OXIDE; PHENOL; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION KINETICS; CHEMICAL STRUCTURE; ELECTROPHILICITY; ENANTIOSELECTIVITY; PROTON TRANSPORT; SUZUKI REACTION;

EID: 84555187026     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja210025q     Document Type: Article

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