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A preparatively convenient ligand-free catalytic PEG 2000 Suzuki-Miyaura coupling.
Razler, Thomas M; Hsiao, Yi; Qian, Feng; Fu, Ruiling; Khan, Rana Kashif; Doubleday, Wendel.
Afiliação
  • Razler TM; Department of Process Research and Development, Bristol-Myers Squibb, One Squibb Drive, New Brunswick, New Jersey 08903, USA. thomas.razler@bms.com
J Org Chem ; 74(3): 1381-4, 2009 Feb 06.
Article em En | MEDLINE | ID: mdl-19178357
ABSTRACT
A ligand-free Suzuki-Miyaura reaction for the cross-coupling of aryl and heteroaryl bromides with aryl and heteroarylboronic acids has been developed utilizing catalytic polyethylene glycol 2000 (PEG 2000). This preparatively convenient system afforded the corresponding cross-coupled products in good to excellent isolated yields after a simple aqueous workup. Transmission electron microscopy (TEM) analysis of the Pd-PEG 2000 catalyst system revealed in situ-generated palladium nanoparticles after only 1 min of reaction.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polietilenoglicóis / Compostos de Bifenilo / Ácidos Borônicos / Bromobenzenos Idioma: En Revista: J Org Chem Ano de publicação: 2009 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polietilenoglicóis / Compostos de Bifenilo / Ácidos Borônicos / Bromobenzenos Idioma: En Revista: J Org Chem Ano de publicação: 2009 Tipo de documento: Article País de afiliação: Estados Unidos