Please use this identifier to cite or link to this item: http://dspace.iitrpr.ac.in:8080/xmlui/handle/123456789/2885
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dc.contributor.authorMishra, K.-
dc.contributor.authorPandey, A. K.-
dc.contributor.authorSingh, J. B.-
dc.contributor.authorSingh, R. M.-
dc.date.accessioned2021-10-04T11:22:00Z-
dc.date.available2021-10-04T11:22:00Z-
dc.date.issued2021-10-04-
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/2885-
dc.description.abstractA metal-free, TBHP-promoted economical route is developed via the sp2 C–H bond functionalization strategy for the synthesis of indenoquinolinones, 4-azafluorenones and fluorenones. Reactions provided excellent yield of the products under mild conditions. We have successfully synthesized 11H-indeno [1,2-b]quinolin-11-one, an antibacterial agent, in excellent yields.en_US
dc.language.isoen_USen_US
dc.titleMetal free TBHP-promoted intramolecular carbonylation of arenes: Via radical cross-dehydrogenative coupling: Synthesis of indenoquinolinones, 4-azafluorenones and fluorenonesen_US
dc.typeArticleen_US
Appears in Collections:Year-2016

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