Palladium-Catalyzed Heck Coupling Reaction of Aryl Bromides in Aqueous Media Using Tetrahydropyrimidinium Salts as Carbene Ligands

An efficient and stereoselective catalytic system for the Heck cross coupling reaction using novel 1,3-dialkyl-3,4,5,6-tetrahydropyrimidinium salts (1, LHX) and Pd(OAc)(2) loading has been reported. The palladium complexes derived from the salts 1a-f prepared in situ exhibit good catalytic activity...

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Detalles Bibliográficos
Autores principales: Yaşar, Sedat, Özcan, Emine Özge, Gürbüz, Nevin, Çetinkaya, Bekir, Özdemir, İsmail
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International 2010
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6263193/
https://www.ncbi.nlm.nih.gov/pubmed/20335935
http://dx.doi.org/10.3390/molecules15020649
Descripción
Sumario:An efficient and stereoselective catalytic system for the Heck cross coupling reaction using novel 1,3-dialkyl-3,4,5,6-tetrahydropyrimidinium salts (1, LHX) and Pd(OAc)(2) loading has been reported. The palladium complexes derived from the salts 1a-f prepared in situ exhibit good catalytic activity in the Heck coupling reaction of aryl bromides under mild conditions.

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