Iridium-catalyzed [4 + 2] annulation of 1-arylindazolones with α-diazo carbonyl compounds: access to indazolone-fused cinnolines

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DC Field	Value	Language
dc.contributor.author	Sakhuja, Rajeev	-
dc.date.accessioned	2021-11-11T10:58:29Z	-
dc.date.available	2021-11-11T10:58:29Z	-
dc.date.issued	2018	-
dc.identifier.uri	https://pubs.rsc.org/en/content/articlelanding/2018/ob/c8ob01681j	-
dc.identifier.uri	http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3350	-
dc.description.abstract	An efficient one-pot Ir-catalyzed method was developed for the synthesis of indazolone-fused cinnolines by [4 + 2] annulation of 1-arylindazolones with α-diazo carbonyl compounds via sequential C–H activation/carbene insertion/cyclization in a tandem manner. This method has excellent tolerance towards electron-withdrawing and electron-donating functional groups on 1-arylindazolone. This method was also found to be applicable to cyclic α-diazo carbonyl compounds.	en_US
dc.language.iso	en	en_US
dc.publisher	RSC	en_US
dc.subject	Chemistry	en_US
dc.subject	Iridium-catalyzed [4 + 2]	en_US
dc.subject	Indazolone-fused cinnolines	en_US
dc.title	Iridium-catalyzed [4 + 2] annulation of 1-arylindazolones with α-diazo carbonyl compounds: access to indazolone-fused cinnolines	en_US
dc.type	Article	en_US
Appears in Collections:	Department of Chemistry

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