Journal
REACTION CHEMISTRY & ENGINEERING
Volume 4, Issue 2, Pages 372-382Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c8re00235e
Keywords
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Funding
- CSIR Parliamentary Grant
- National Research Foundation (NRF, South Africa) Thuthuka grant [106959]
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An immobilized triphenylphosphine scaffold was prepared by precipitation polymerization and functionalized to afford a cost-effective source of solid-supported tetrakis(triphenylphosphine)palladium(0). The catalyst was characterised and used to perform biphasic Suzuki-Miyaura cross-coupling reactions using a packed-bed reactor under flow conditions. The approach afforded comparable yields to those obtained under batch conditions with a single pass through the packed-bed reactor (1 h vs. 18 h). The use of a recycling system was investigated on a model reaction and found to afford close to quantitative conversion within 3 hours.
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