PdII-catalyzed highly selective arylation of allyl esters via C-H functionalization of unreactive arenes with retention of the traditional leaving group

Chemistry - An Asian Journal

Volumn 5, Issue 5, 2010, Pages 1090-1093

  Pan, Delin ^a   Yu, Miao ^b   Chen, Wei ^c   Jiao, Ning ^a  

^a PEKING UNIVERSITY HEALTH SCIENCE CENTER   (China)

^b CHINESE PLA GENERAL HOSPITAL   (China)

^c MEDICAL SCHOOL OF CHINESE PLA   (China)

Author keywords

Allylic compounds; Heck reaction; Palladium; Regioselectivity; Silver

Indexed keywords

ALLYLIC COMPOUNDS; ARYLATIONS; C-H ACTIVATION; C-H FUNCTIONALIZATION; CH-BOND ACTIVATION; ELECTRON-DEFICIENT; HECK REACTION; HECK REACTIONS; LEAVING GROUPS; STEREO-SELECTIVE;

ACTIVATION ANALYSIS; AROMATIC COMPOUNDS; CHEMICAL BONDS; ESTERIFICATION; PALLADIUM; REGIOSELECTIVITY; SILVER;

ESTERS;

ACETIC ACID DERIVATIVE; ALLYL ACETATE; ALLYL COMPOUND; BENZENE; CARBON; ESTER; PALLADIUM;

ARTICLE; CATALYSIS; CHEMISTRY; OXIDATION REDUCTION REACTION; STEREOISOMERISM;

ACETATES; ALLYL COMPOUNDS; BENZENE; CARBON; CATALYSIS; ESTERS; OXIDATION-REDUCTION; PALLADIUM; STEREOISOMERISM;

EID: 77951874098     PISSN: 18614728     EISSN: 1861471X     Source Type: Journal    
DOI: 10.1002/asia.200900558     Document Type: Article

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