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Highly Efficient Method for Suzuki Reactions in Aqueous Media

[Image: see text] Herein, we report the crystal structure and characterization of mono-6-(l-aminopropanol)-deoxy-β-cyclodextrin (L(n)@β-CD). A highly efficient, in situ generated catalyst, PdCl(2)(L(n)@β-CD), was synthesized for palladium-catalyzed cross-coupling reactions under mild reaction condit...

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Detalles Bibliográficos
Autores principales: Zhou, Xinglong, Guo, Xuming, Jian, Fangfang, Wei, Gang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2018
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6641778/
https://www.ncbi.nlm.nih.gov/pubmed/31458668
http://dx.doi.org/10.1021/acsomega.8b00469
Descripción
Sumario:[Image: see text] Herein, we report the crystal structure and characterization of mono-6-(l-aminopropanol)-deoxy-β-cyclodextrin (L(n)@β-CD). A highly efficient, in situ generated catalyst, PdCl(2)(L(n)@β-CD), was synthesized for palladium-catalyzed cross-coupling reactions under mild reaction conditions, and the use of this catalyst in Suzuki cross-couplings was investigated. Low palladium loadings of 0.01 mol % PdCl(2)(L(n)@β-CD) (Pd accounted for approximately 8.4% of the catalyst by mass) were found to be highly efficient for Suzuki cross-couplings in water and afforded the corresponding biaryl compounds in excellent yields. The catalyst can be recycled and reused.