Journal
RSC ADVANCES
Volume 5, Issue 25, Pages 19630-19637Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c4ra16677a
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Funding
- Ministry of Education Malaysia [RDU140124]
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An MCM-48 supported 2-pyridinylmethanimine Pd-catalyst was found to be a highly efficient catalyst in the Mizoroki-Heck, Suzuki-Miyaura and copper-free Sonogashira cross-coupling reactions of aryl halides under aqueous reaction conditions. The catalyst efficiently promoted these coupling reactions with ppm levels of palladium to afford the corresponding coupling products in up to 98% yield. The supported Pd-catalyst was readily recovered and reused several times without significant loss of its catalytic activity.
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