Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/2253
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dc.contributor.authorMandal, S.K.-
dc.date.accessioned2020-11-26T06:13:00Z-
dc.date.available2020-11-26T06:13:00Z-
dc.date.issued2018-
dc.identifier.citationOrganic and Biomolecular Chemistry, 16(17), pp. 3220-3228en_US
dc.identifier.otherhttps://doi.org/10.1039/C8OB00586A-
dc.identifier.urihttps://pubs.rsc.org/en/content/articlelanding/2018/ob/c8ob00586a#!divAbstract-
dc.identifier.urihttp://hdl.handle.net/123456789/2253-
dc.descriptionOnly IISERM authors are available in the record.-
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.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectAromatic compoundsen_US
dc.subjectChemical bondsen_US
dc.subjectFused pyrimidineen_US
dc.subjectBenzylaminesen_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
Appears in Collections:Research Articles

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