Abstract
AbstractQuinazolines, particularly fluoro-quinazolines, represent important structural motifs in bioactive molecules and pharmaceuticals. Despite several known synthetic routes, the efficient synthesis of fluorine-containing quinazolines remains a challenge. Herein, the straightforward and sustainable synthesis of fluorine-substituted quinazolines using domino sequences is reported. The obtained novel fluoro-quinazoline compounds exhibit significant in vitro activity against human cytomegalovirus (HCMV), expanding the library of potential antiviral drug compounds. Our finding outlays the synthetic toolkit for fluoro-quinazolines and introduces new agents for HCMV therapy.
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