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DC Field | Value | Language |
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dc.contributor.author | Yadav, Anubha | en_US |
dc.contributor.author | Banerjee, Joyanta | en_US |
dc.contributor.author | Mobin, Shaikh M. | en_US |
dc.contributor.author | Samanta, Sampak | en_US |
dc.date.accessioned | 2022-03-17T01:00:00Z | - |
dc.date.accessioned | 2022-03-21T11:30:39Z | - |
dc.date.available | 2022-03-17T01:00:00Z | - |
dc.date.available | 2022-03-21T11:30:39Z | - |
dc.date.issued | 2018 | - |
dc.identifier.citation | Yadav, 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.201800240 | en_US |
dc.identifier.issn | 2193-5807 | - |
dc.identifier.other | EID(2-s2.0-85051423061) | - |
dc.identifier.uri | https://doi.org/10.1002/ajoc.201800240 | - |
dc.identifier.uri | https://dspace.iiti.ac.in/handle/123456789/9013 | - |
dc.description.abstract | The 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, Weinheim | en_US |
dc.language.iso | en | en_US |
dc.publisher | Wiley-VCH Verlag | en_US |
dc.source | Asian Journal of Organic Chemistry | en_US |
dc.title | Lewis-Base-Catalyzed Domino Reaction of Morita–Baylis–Hillman Carbonates of Isatins with Enolizable Cyclic Carbonyl Compounds: Stereoselective Access to Spirooxindole-Pyrans | en_US |
dc.type | Journal Article | en_US |
Appears in Collections: | Department of Chemistry |
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