Chemoselective Heck arylation of acrolein diethyl acetal catalyzed by an oxime-derived palladacycle

Tetrahedron

Volumn 61, Issue 41, 2005, Pages 9688-9695

  Nájera, Carmen ^a   Botella, Luis ^a  

^a UNIVERSITY OF ALICANTE   (Spain)

Author keywords

3 Arylpropanoates acrolein; Cinnamaldehydes; Heck reaction; Palladacycles

Indexed keywords

(DICYCLOHEXYL)METHYLAMINE; 3 BENZYLOXYCINNAMALDEHYDE; 4 (DIMETHYLAMINO)CINNAMALDEHYDE; 4 HYDROXYACETAPHENONE OXIME; ACROLEIN DERIVATIVE; ACROLEIN DIETHYL ACETAL; CINNAMALDEHYDE DERIVATIVE; DIMER; METHYLAMINE; N,N DIMETHYLACETAMIDE; OXIME; PALLADIUM ACETATE; PALLADIUM COMPLEX; POLYCYCLIC AROMATIC HYDROCARBON DERIVATIVE; POTASSIUM CHLORIDE; POTASSIUM DERIVATIVE; PROPIONIC ACID DERIVATIVE; TETRABUTYLAMMONIUM; TETRABUTYLAMMONIUM ACETATE; UNCLASSIFIED DRUG;

ARTICLE; ARYLATION; CATALYSIS; CATALYST; DRUG ACTIVITY; DRUG POTENCY; DRUG STRUCTURE; DRUG SYNTHESIS; HECK REACTION; HIGH TEMPERATURE PROCEDURES; MICROWAVE IRRADIATION; PRIORITY JOURNAL; REACTION TIME;

EID: 24344450869     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2005.06.059     Document Type: Article

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