Synthesis of biaryl-styrene monomers by microwave-assisted Suzuki coupling
โ Scribed by Hazit A. Zayas; Michael C. Bowyer; Christopher P. Gordon; Clovia I. Holdsworth; Adam McCluskey
- Book ID
- 104096829
- Publisher
- Elsevier Science
- Year
- 2009
- Tongue
- French
- Weight
- 210 KB
- Volume
- 50
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
a b s t r a c t Biaryl-styrenic monomers are prepared via Suzuki coupling as functional monomers in the synthesis of molecularly imprinted polymers. Traditional thermal Suzuki approaches are hampered by competition between Suzuki, Heck and homo-coupling reactions. Microwave-assisted approaches facilitated rapid access to the desired Suzuki products whilst suppressing both Heck and homo-couplings of 4-vinylboronic acid.
๐ SIMILAR VOLUMES
## Abstract A protocol for the microwaveโassisted decarboxylative crossโcouplings of carboxylic acid salts with aryl halides has been developed that allows the synthesis of various biaryls and aryl ketones in high yields. After careful adaptation of the bimetallic catalyst system and reaction condi
A range of conjugated polyaryls has been synthesized through one-pot microwave assisted palladium-catalyzed consecutive Suzuki coupling reactions on a KF-alumina surface with notable features including rapid reaction times, solvent-free conditions, high yields, atom economic and air-insensitive reac