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

Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/2220

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DC Field	Value	Language
dc.contributor.author	Markad, D.	-
dc.contributor.author	Mandal, S.K.	-
dc.date.accessioned	2020-11-25T11:11:35Z	-
dc.date.available	2020-11-25T11:11:35Z	-
dc.date.issued	2018	-
dc.identifier.citation	Organic and Biomolecular Chemistry, 16(44), pp. 8585-8595	en_US
dc.identifier.other	https://doi.org/10.1039/C8OB01681J	-
dc.identifier.uri	https://pubs.rsc.org/en/content/articlelanding/2018/ob/c8ob01681j#!divAbstract	-
dc.identifier.uri	http://hdl.handle.net/123456789/2220	-
dc.description	Only IISERM authors are available in the record.	-
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	Royal Society of Chemistry	en_US
dc.subject	Carbonyl compounds	en_US
dc.subject	Electron-donating	en_US
dc.subject	Activation analysis	en_US
dc.subject	Iridium	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:	Research Articles

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