Combining the use of solid-supported transition metal catalysis with microwave irradiation in solution-phase parallel library synthesis
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Updated: Aug 27, 2026

A Microwave-Assisted Direct Heteroarylation of Ketones Using Transition Metal Catalysis
Published on: February 16, 2020
Michael G Organ1, Stanislas Mayer, Franck Lepifre
1The Department of Chemistry York University, 4700 Keele Street, Toronto, Ontario, Canada, M3J 1P3. organ@yorku.ca
Abstract:
Microwave heating methods have been combined with the use of solid-supported catalysts to produce small solution-phase libraries of medicinally-relevant compounds. Palladium supported on charcoal (Pd/C) has been used to produce libraries of pyrazole compounds for screening in COX II studies via Suzuki cross coupling reactions, while the same catalyst has been used also to produce styryl-based nAChR compounds using analogous chemistry. Although the reaction substrates are very different (aryl vs. vinyl), this catalyst system provided consistently good and reliable results. The use of a polystyrene-supported Ru catalyst for ring-closing metathesis (RCM) reactions was also evaluated to prepare benzolactam structures for evaluation as factor Xa inhibitors.

