Suzuki–Miyaura reactions in PEG–water solutions using Pd/BaSO 4  as catalytic source | Zendy

de Souza Andréa Luzia F. | Zendy; Silva Aires da Conceição | Zendy; Antunes O. A. C. | Zendy

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Suzuki–Miyaura reactions in PEG–water solutions using Pd/BaSO 4 as catalytic source

Author(s) -

de Souza Andréa Luzia F.,

Silva Aires da Conceição,

Antunes O. A. C.

Publication year - 2009

Publication title -

applied organometallic chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.53

H-Index - 71

eISSN - 1099-0739

pISSN - 0268-2605

DOI - 10.1002/aoc.1455

Subject(s) - chemistry , catalysis , peg ratio , catalytic cycle , ligand (biochemistry) , combinatorial chemistry , phenylboronic acid , organic chemistry , polymer chemistry , biochemistry , receptor , finance , economics

Suzuki–Miyaura reactions between halobenzenes and other substituted (hetero)arenes and boronic acids were carried out in PEG–water solution using Pd/BaSO 4 as catalytic source in a ligand‐free system. High to moderate yields were generally obtained. The catalytic system could be recycled up to six times, showing a slight decrease in activity after each cycle. Copyright © 2008 John Wiley & Sons, Ltd.

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