6533b85bfe1ef96bd12bb653

RESEARCH PRODUCT

Palladium-catalyzed reaction of boronic acids with chiral and racemic alpha-bromo sulfoxides.

Carmen Ramírez De ArellanoAna B. CuencaGregorio AsensioDenissa PeineMercedes Medio-simónNuria Rodriguez

subject

chemistry.chemical_classificationReaction mechanismAqueous solutionBase (chemistry)Organic ChemistrySide reactionchemistry.chemical_elementSulfoxideMedicinal chemistryCatalysischemistry.chemical_compoundchemistryRacemizationPalladium

description

Palladium-catalyzed cross-coupling reactions of racemic alpha-bromo sulfoxides with boronic acids are carried out in either aqueous or nonaqueous medium with formation of a new C sp(3)-C sp(2) bond. The arylation of chiral alpha-bromo sulfoxides occurs without racemization. The cross-coupling reaction is general and gives high yields with arylboronic acids substituted with either donor or acceptor groups but gives poor results with heteroarylboronic acids. The best yields are obtained using degassed solvents and CsF instead of aqueous base. The use of aqueous base and the presence of oxygen favor the homocoupling side reaction.

10.1021/jo0487552https://pubmed.ncbi.nlm.nih.gov/15527292