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Highly Efficient Method for Suzuki Reactions in Aqueous Media
Author(s) -
Xinglong Zhou,
Xuming Guo,
FangFang Jian,
Gang Wei
Publication year - 2018
Publication title -
acs omega
Language(s) - English
Resource type - Journals
ISSN - 2470-1343
DOI - 10.1021/acsomega.8b00469
Subject(s) - catalysis , palladium , aqueous medium , suzuki reaction , aqueous solution , chemistry , coupling reaction , polymer chemistry , combinatorial chemistry , organic chemistry
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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