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Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/16402
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dc.contributor.authorSermadurai, Selvakumaren_US
dc.date.accessioned2025-07-09T13:48:00Z-
dc.date.available2025-07-09T13:48:00Z-
dc.date.issued2025-
dc.identifier.citationKumari, A., Jain, A., Sharma, H., Sermadurai, S., & Rana, N. K. (2025). Catalyst-free efficient synthesis of functionalized 1,2,4-triazole via ring opening/cyclization of arylidene thiazolone with aryl/alkyl-hydrazine. Chemical Communications. https://doi.org/10.1039/d5cc02145fen_US
dc.identifier.issn1359-7345-
dc.identifier.otherEID(2-s2.0-105008648037)-
dc.identifier.urihttps://dx.doi.org/10.1039/d5cc02145f-
dc.identifier.urihttps://dspace.iiti.ac.in:8080/jspui/handle/123456789/16402-
dc.description.abstractWe report a catalyst-free synthesis of hydrazone-substituted 1,2,4-triazoles via ring opening/intramolecular cyclization of arylidene thiazolone by aryl/alkyl-hydrazine. The reaction exhibits a broad substrate scope and is demonstrated on a gram scale in both batch and continuous flow synthesis. Furthermore, the direct one-pot synthesis of indole-substituted 1,2,4-triazole expands its structural diversity. © 2025 The Royal Society of Chemistry.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.sourceChemical Communicationsen_US
dc.titleCatalyst-free efficient synthesis of functionalized 1,2,4-triazole via ring opening/cyclization of arylidene thiazolone with aryl/alkyl-hydrazineen_US
dc.typeJournal Articleen_US
Appears in Collections:Department of Chemistry

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