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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/15501
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dc.contributor.authorKumar, Anil-
dc.contributor.authorSakhuja, Rajeev-
dc.date.accessioned2024-09-10T06:45:16Z-
dc.date.available2024-09-10T06:45:16Z-
dc.date.issued2022-11-
dc.identifier.urihttps://onlinelibrary.wiley.com/doi/abs/10.1002/9783527834242.chf0113-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/15501-
dc.description.abstractThe indazole is an important class of bicyclic nitrogen-containing heterocycle that forms the core structure of a large number of compounds with potential therapeutic value. Consequently, CH functionalization of this scaffold has been extensively explored using transition metal-catalyzed and metal-free CH functionalization strategies. This article provides a perspective on various strategies that have been developed to add a substituent on this heterocycle core and their appropriate coupling partners.en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.subjectChemistryen_US
dc.subjectHeterocyclesen_US
dc.subjectIndazoleen_US
dc.titleC--H Functionalization of Indazolesen_US
dc.typeBook chapteren_US
Appears in Collections:Department of Chemistry

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