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	Mandal, Sanjay K.	-
dc.date.accessioned	2023-08-22T11:17:24Z	-
dc.date.available	2023-08-22T11:17:24Z	-
dc.date.issued	2021	-
dc.identifier.citation	The Journal of Organic Chemistry, 86(3), 2734–2747.	en_US
dc.identifier.uri	https://pubs.acs.org/doi/10.1021/acs.joc.0c02729	-
dc.identifier.uri	http://hdl.handle.net/123456789/5022	-
dc.description	Only IISER Mohali authors are available in the record.	en_US
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_US	en_US
dc.publisher	ACS Publications	en_US
dc.subject	Purification	en_US
dc.subject	Organic compounds	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:	Research Articles

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