Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/11877
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dc.contributor.authorRani, Poonamen_US
dc.contributor.authorPrakash, Meheren_US
dc.contributor.authorSamanta, Sampaken_US
dc.date.accessioned2023-06-20T15:34:06Z-
dc.date.available2023-06-20T15:34:06Z-
dc.date.issued2023-
dc.identifier.citationRani, P., Prakash, M., & Samanta, S. (2023). Organobase-catalyzed mannich reaction of cyclic N-sulfonyl imines and 1,2-diketones: A sustainable approach to 4-(3-arylquinoxalin-2-ylmethyl)sufamidates. Tetrahedron Letters, 122 doi:10.1016/j.tetlet.2023.154490en_US
dc.identifier.issn0040-4039-
dc.identifier.otherEID(2-s2.0-85152267120)-
dc.identifier.urihttps://doi.org/10.1016/j.tetlet.2023.154490-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/11877-
dc.description.abstractA convenient, eco-friendly, organobase-catalyzed one-pot two-step sequential approach to a fascinating class of various 4-(3-arylquinoxalin-2-ylmethyl)-substituted sulfamidates in good to high yields is reported. This C–C/C[dbnd]N bond-forming reaction proceeds via a Mannich reaction of cyclic N-sulfonyl aldimines with 1-aryl-2-alkyl-1,2-diketones catalyzed by triethylamine, followed by the aza-cyclization of in situ formed 1,2-dicarbonyl precursors with ortho-diaminoarenes in PEG-400 as a natural, reusable, and benign solvent at room temperature. In addition, this 100% carbon atom-economic approach could be viable for gram-scale synthesis and tolerates various synthetically resourceful functionalities under mild conditions. © 2023 Elsevier Ltden_US
dc.language.isoenen_US
dc.publisherElsevier Ltden_US
dc.sourceTetrahedron Lettersen_US
dc.subject4-(3-Arylquinoxalin-2-ylmethyl)-substituted sulfamidatesen_US
dc.subjectCyclic N-sulfonyl iminesen_US
dc.subjectGreen methoden_US
dc.subjectMannich reactionen_US
dc.subjectOrganobase-catalyzeden_US
dc.titleOrganobase-catalyzed Mannich reaction of cyclic N-sulfonyl imines and 1,2-diketones: A sustainable approach to 4-(3-arylquinoxalin-2-ylmethyl)sufamidatesen_US
dc.typeJournal Articleen_US
Appears in Collections:Department of Mathematics

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