Palladium-catalysed Heck-type alkenylation reactions in the synthesis of quinolines. Mechanistic insights and recent applications
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Date
2020-05-18Author
Carral Menoyo, Asier
Sotomayor Anduiza, María Nuria
Lete Expósito, María Esther
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Catalysis Science & Technology 10 : 5345-5361(2020)
Abstract
Quinoline and quinolone cores are present in a wide variety of pharmaceuticals, agrochemicals and materials, as well in ligands/catalysts in asymmetric synthesis. Transition-metal catalysed based approaches have played a pivotal role in the development of the catalytic methods for their synthesis. This review presents recent developments on palladiumcatalysed Mizoroki-Heck reaction and its dehydrogenative variant (the Fujiwara-Moritani reaction), a C-H activation reaction that does not require the use of prefunctionalized coupling parterns for the synthesis of quinoline frameworks. The mechanistic understanding of both type of reactions, and how the different reaction conditions affect the outcome and the regioselectivity for the synthesis of the quinoline core, which is crucial to achieve target-oriented synthesis successfully, is discussed through selected examples.