Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/8860
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dc.contributor.authorYadav, Anubhaen_US
dc.contributor.authorGudimella, Santosh K.en_US
dc.contributor.authorSamanta, Sampaken_US
dc.date.accessioned2022-03-17T01:00:00Z-
dc.date.accessioned2022-03-21T11:30:03Z-
dc.date.available2022-03-17T01:00:00Z-
dc.date.available2022-03-21T11:30:03Z-
dc.date.issued2019-
dc.identifier.citationYadav, A., Gudimella, S. K., & Samanta, S. (2019). An expedient lewis-acid-catalyzed microwave-assisted domino approach to coumarin-fused pyrroles and related heterocycles under neat conditions. ChemistrySelect, 4(43), 12768-12773. doi:10.1002/slct.201903711en_US
dc.identifier.issn2365-6549-
dc.identifier.otherEID(2-s2.0-85075614103)-
dc.identifier.urihttps://doi.org/10.1002/slct.201903711-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/8860-
dc.description.abstractA superior Lewis acid-catalyzed and microwave-assisted, facile, solvent-free, one-pot quick access to a novel class of a set of diversely substituted coumarin, dimedone and naphthoquinone-fused pyrroles via an annulation reaction between different kinds of carbo-and heterocyclic enaminones and a group of α-aroyl/heteroaryl/acetylidene malonates, 3-aroylidene-2-oxindoles is reported. This LUMO-lowering technique involving a powerful Lewis acid relies on the installation of pyrrole rings good to high chemical yields with a wide scope of diversely substituted substances. Furthermore, a direct C(sp3)-H hydroxylation of 3-pyrrolocoumarinyl-2-oxindoles to therapeutically exciting 3-hydroxy-3-pyrrolocoumarinyl-2-oxindoles bearing a tetra-substituted chiral carbon center in high yields was achieved under metal-free conditions. © 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheimen_US
dc.language.isoenen_US
dc.publisherWiley-Blackwellen_US
dc.sourceChemistrySelecten_US
dc.titleAn Expedient Lewis-Acid-Catalyzed Microwave-Assisted Domino Approach to Coumarin-Fused Pyrroles and Related Heterocycles under Neat Conditionsen_US
dc.typeJournal Articleen_US
Appears in Collections:Department of Chemistry

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