Reducing-Agent-Free Convergent Synthesis of Hydroxyimino-Decorated Tetracyclic Fused Cinnolines via RhIII-Catalyzed Annulation Using Nitroolefins

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DC Field	Value	Language
dc.contributor.author	Sakhuja, Rajeev	-
dc.date.accessioned	2021-11-11T10:57:56Z	-
dc.date.available	2021-11-11T10:57:56Z	-
dc.date.issued	2021-01	-
dc.identifier.uri	https://pubs.acs.org/doi/10.1021/acs.joc.0c02729	-
dc.identifier.uri	http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3342	-
dc.description.abstract	A mild Rh-catalyzed method was developed for the synthesis of hydroxyimino functionalized indazolo[1,2-a]cinnolines and phthalazino[2,3-a]cinnolines by reductive [4 + 2] annulation between 1-arylindazolones and 2-aryl-2,3-dihydrophthalazine-1,4-diones with varied nitroolefins. The targeted oxime decorated tetracyclic fused cinnolines were synthesized via sequential C–H activation/olefin insertion/reduction under reducing-agent-free conditions.	en_US
dc.language.iso	en	en_US
dc.publisher	ACS	en_US
dc.subject	Chemistry	en_US
dc.subject	Annulations	en_US
dc.subject	H2 Purification	en_US
dc.subject	Organic compounds	en_US
dc.subject	Column chromatography	en_US
dc.subject	Ethanol	en_US
dc.title	Reducing-Agent-Free Convergent Synthesis of Hydroxyimino-Decorated Tetracyclic Fused Cinnolines via RhIII-Catalyzed Annulation Using Nitroolefins	en_US
dc.type	Article	en_US
Appears in Collections:	Department of Chemistry

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