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DC Field | Value | Language |
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dc.contributor.author | Yadav, Anubha | en_US |
dc.contributor.author | Gudimella, Santosh K. | en_US |
dc.contributor.author | Samanta, Sampak | en_US |
dc.date.accessioned | 2022-03-17T01:00:00Z | - |
dc.date.accessioned | 2022-03-21T11:30:03Z | - |
dc.date.available | 2022-03-17T01:00:00Z | - |
dc.date.available | 2022-03-21T11:30:03Z | - |
dc.date.issued | 2019 | - |
dc.identifier.citation | Yadav, 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.201903711 | en_US |
dc.identifier.issn | 2365-6549 | - |
dc.identifier.other | EID(2-s2.0-85075614103) | - |
dc.identifier.uri | https://doi.org/10.1002/slct.201903711 | - |
dc.identifier.uri | https://dspace.iiti.ac.in/handle/123456789/8860 | - |
dc.description.abstract | A 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, Weinheim | en_US |
dc.language.iso | en | en_US |
dc.publisher | Wiley-Blackwell | en_US |
dc.source | ChemistrySelect | en_US |
dc.title | An Expedient Lewis-Acid-Catalyzed Microwave-Assisted Domino Approach to Coumarin-Fused Pyrroles and Related Heterocycles under Neat Conditions | en_US |
dc.type | Journal Article | en_US |
Appears in Collections: | Department of Chemistry |
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