Effect of the substituent position on the enantioselective hydrogenation of methoxy-substituted 2,3-diphenylpropenoic acids over palladium catalyst

Journal of Molecular Catalysis A: Chemical

Volumn 290, Issue 1-2, 2008, Pages 54-59

  Szollosi, György ^a   Hermán, Beáta ^b   Felföldi, Károly ^a   Fülöp, Ferenc ^a,b   Bartók, Mihály ^a  

^a UNIVERSITY OF SZEGED   (Hungary)

^b UNIVERSITY OF SZEGED   (Hungary)

Author keywords

(E) 2,3 Diphenylpropenoic acid; Benzylamine; Cinchonidine; Enantioselective; Hydrogenation; Methoxy substituent; Palladium; Substituent position

Indexed keywords

ACIDS; CATALYSIS; ENANTIOSELECTIVITY; PALLADIUM; PHOTOACOUSTIC EFFECT; RATE CONSTANTS; REACTION RATES;

ELECTRONIC EFFECTS; ELSEVIER (CO); ENANTIOSELECTIVE HYDROGENATION; ENANTIOSELECTIVITIES; METHOXY; PALLADIUM CATALYSTS; PHENYL RINGS; STERIC EFFECTS; SUBSTITUTED DERIVATIVES; SUPPORTED PD;

HYDROGENATION;

EID: 46149127069     PISSN: 13811169     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.molcata.2008.05.004     Document Type: Article

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