advances in metal-catalyzed cross-coupling reactions of halogenated quinazolinones and their quinazoline derivatives

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ID: 143459
2014
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Abstract
Halogenated quinazolinones and quinazolines are versatile synthetic intermediates for the metal-catalyzed carbon–carbon bond formation reactions such as the Kumada, Stille, Negishi, Sonogashira, Suzuki-Miyaura and Heck cross-coupling reactions or carbon-heteroatom bond formation via the Buchwald-Hartwig cross-coupling to yield novel polysubstituted derivatives. This review presents an overview of the application of these methods on halogenated quinazolin-4-ones and their quinazolines to generate novel polysubstituted derivatives.
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mphahlele2014moleculesadvances Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors ;Malose Jack Mphahlele;Marole Maria Maluleka
Journal Journal of ethnopharmacology
Year 2014
DOI
10.3390/molecules191117435
URL
http://www.mdpi.com/1420-3049/19/11/17435
Keywords Keywords not found

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