Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/9013
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dc.contributor.authorYadav, Anubhaen_US
dc.contributor.authorBanerjee, Joyantaen_US
dc.contributor.authorMobin, Shaikh M.en_US
dc.contributor.authorSamanta, Sampaken_US
dc.date.accessioned2022-03-17T01:00:00Z-
dc.date.accessioned2022-03-21T11:30:39Z-
dc.date.available2022-03-17T01:00:00Z-
dc.date.available2022-03-21T11:30:39Z-
dc.date.issued2018-
dc.identifier.citationYadav, A., Banerjee, J., Arupula, S. K., Mobin, S. M., & Samanta, S. (2018). Lewis-base-catalyzed domino reaction of Morita–Baylis–Hillman carbonates of isatins with enolizable cyclic carbonyl compounds: Stereoselective access to spirooxindole-pyrans. Asian Journal of Organic Chemistry, 7(8), 1595-1599. doi:10.1002/ajoc.201800240en_US
dc.identifier.issn2193-5807-
dc.identifier.otherEID(2-s2.0-85051423061)-
dc.identifier.urihttps://doi.org/10.1002/ajoc.201800240-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/9013-
dc.description.abstractThe present paper reports an efficient, organocatalytic, environmentally friendly and stereoselective [3+3] one-pot allylic alkylation/oxa-Michael reaction by involving a wide range of Morita–Baylis–Hillman (MBH) carbonates of isatins and several pharmacologically attractive enolizable C−H activated cyclic carbonyl compounds such as 1,3-binucleophiles, namely pyrazolones, isoxazolones, 4-hydroxyxoumarins, 4-hydroxy-6-methyl-α-pyrone, lawsone and dimedone in a biomass-derived 2-MeTHF as green solvent catalyzed by DABCO as a solid Lewis-base catalyst. This protocol delivers a unique class of medicinally promising spirooxindole-fused-dihydropyran scaffolds. © 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheimen_US
dc.language.isoenen_US
dc.publisherWiley-VCH Verlagen_US
dc.sourceAsian Journal of Organic Chemistryen_US
dc.titleLewis-Base-Catalyzed Domino Reaction of Morita–Baylis–Hillman Carbonates of Isatins with Enolizable Cyclic Carbonyl Compounds: Stereoselective Access to Spirooxindole-Pyransen_US
dc.typeJournal Articleen_US
Appears in Collections:Department of Chemistry

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