1. IDR@IIT Indore
  2. IITI Scholarly Publications
  3. Department of Chemistry
Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/15997
Full metadata record
DC FieldValueLanguage
dc.contributor.authorChillal, Abhinay Subodhen_US
dc.contributor.authorKumari, Varshaen_US
dc.contributor.authorKshirsagar, Umesh Achyutraoen_US
dc.date.accessioned2025-04-28T12:48:02Z-
dc.date.available2025-04-28T12:48:02Z-
dc.date.issued2025-
dc.identifier.citationChillal, A. S., Kumari, V., & Kshirsagar, U. A. (2025). NIS-promoted carbochalcogenation of styrenes: regioselective C-3 alkylation of pyrazolo[1,5-a]pyrimidines. Organic and Biomolecular Chemistry. https://doi.org/10.1039/d5ob00303ben_US
dc.identifier.issn1477-0520-
dc.identifier.otherEID(2-s2.0-105002766219)-
dc.identifier.urihttps://doi.org/10.1039/d5ob00303b-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/15997-
dc.description.abstractAn N-iodosuccinimide (NIS) mediated transition metal and solvent-free, regioselective multicomponent cascade reaction is developed for the C-3 alkylation of pyrazolo[1,5-a]pyrimidines via a three-component reaction of styrenes, diaryl dichalcogenides and pyrazolo[1,5-a]pyrimidines. This operationally simple, cost-effective and rapid reaction furnishes C-3 functionalized pyrazolo[1,5-a]pyrimidines in good to excellent yields. The reaction is scalable and operates via an electrophilic substitution mechanism. © 2025 The Royal Society of Chemistry.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.sourceOrganic and Biomolecular Chemistryen_US
dc.titleNIS-promoted carbochalcogenation of styrenes: regioselective C-3 alkylation of pyrazolo[1,5-a]pyrimidinesen_US
dc.typeJournal Articleen_US
Appears in Collections:Department of Chemistry

Files in This Item:
There are no files associated with this item.
Show simple item record


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

Altmetric Badge: