An efficient synthesis of chalcones based on the Suzuki reaction

Tetrahedron Letters

Volumn 44, Issue 28, 2003, Pages 5359-5363

  Eddarir, Said ^a,b   Cotelle, Nicole ^a   Bakkour, Youssef ^a   Rolando, Christian ^a  

^a UNIV LILLE   (France)

^b FACULTÉ DES SCIENCES ET TECHNIQUES GUÉLIZ   (Morocco)

Author keywords

[No Author keywords available]

Indexed keywords

3',4,4' TRIMETHOXYCHALCONE; BORONIC ACID DERIVATIVE; CHALCONE DERIVATIVE; CHLORIDE; CINNAMIC ACID DERIVATIVE; UNCLASSIFIED DRUG; VINYL DERIVATIVE;

ARTICLE; DRUG SYNTHESIS; METHODOLOGY;

LATEOLABRAX JAPONICUS;

EID: 0038684441     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(03)01140-7     Document Type: Article

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44. 13C NMR). All boronic acids and acyl chlorides were from commercial sources, and used without further purification except p-methoxy-phenylvinylboronic acid synthesized as described below.
45. 4, and concentrated in vacuo giving 193 mg (yield 92%) of E-2-(4-methoxyphenyl)ethenylboronic acid.