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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2018
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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 |
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. |
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