A convenient palladium/ligand catalyst for Suzuki cross-coupling reactions of arylboronic acids and aryl chlorides

Tetrahedron Letters

Volumn 40, Issue 20, 1999, Pages 3855-3858

  Xiaohong, Bei ^a   Crevier, Thomas ^a   Guram, Anil S ^a   Jandeleit, Bernd ^a   Powers, Timothy S ^a   Turner, Howard W ^a   Uno, Tetsuo ^a   Weinberg, W Henry ^a  

^a SYMYX TECHNOLOGIES   (United States)

Author keywords

Aryl chloride; Arylboronic acid; Catalysis; Palladium; Phosphine

Indexed keywords

BORONIC ACID DERIVATIVE; CHLORIDE; PALLADIUM; PHOSPHINE;

ARTICLE; CATALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; MOLECULAR STABILITY; SYNTHESIS;

EID: 0033553556     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(99)00642-5     Document Type: Article

References (29)

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27. 4, filtered and concentrated in vacua. The crude product was purified by column chromatography on silica gel to afford desired biaryl product, after drying under vacuum.
28. 8 Bei, X.; Uno, T. Norris, J.; Turner, H. W.; Weinberg, W. H.; Guram, A. S.; Petersen, J. L. Organometallics, 1999, in press.
29. 3 ligand (ref. 4b), although commercially available, is not convenient to use due to its potentially pyrophoric nature.