An unprecedented tandem synthesis of fluorescent coumarin-fused pyrimidines via copper-catalyzed cross-dehydrogenative C(sp3)–N bond coupling

dc.contributor.authorSakhuja, Rajeev
dc.date.accessioned2021-11-11T10:58:46Z
dc.date.available2021-11-11T10:58:46Z
dc.date.issued2018
dc.description.abstractAn efficient, one-pot Cu-catalyzed tandem synthesis of fluorescent 1-benzyl-2-phenyl-1,2-dihydro-5H-chromeno[4,3-d]pyrimidin-5-ones from 4-chloro-3-formylcoumarin and benzylamines was developed by in situ intramolecular cross-dehydrogenative C(sp3)–N bond formation in moderate-to-good yields under ligand-free ambient conditions. This synthesis was easily scalable, and the generality of the substrates was established. These coumarin-fused pyrimidines exhibited interesting photo-physical properties and high quantum yields, and would be potential candidates for facilitating suitable studies in medicinal chemistry and materials science.en_US
dc.identifier.urihttps://pubs.rsc.org/en/content/articlelanding/2018/ob/c8ob00586a
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3354
dc.language.isoenen_US
dc.publisherRSCen_US
dc.subjectChemistryen_US
dc.subjectSynthesisen_US
dc.subjectFluorescent coumarin-fuseden_US
dc.subjectPyrimidines via copper-catalyzeden_US
dc.titleAn unprecedented tandem synthesis of fluorescent coumarin-fused pyrimidines via copper-catalyzed cross-dehydrogenative C(sp3)–N bond couplingen_US
dc.typeArticleen_US

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