Weak Chelating Group Directed Palladium-catalyzed C-4 Arylation of Indoles

Please use this identifier to cite or link to this item: http://hdl.handle.net/2080/4386

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DC Field	Value	Language
dc.contributor.author	Gupta, Sandip Kumar	-
dc.contributor.author	Panda, Niranjan	-
dc.date.accessioned	2024-02-13T10:42:34Z	-
dc.date.available	2024-02-13T10:42:34Z	-
dc.date.issued	2024-01	-
dc.identifier.citation	37th Annual Conference of Orissa Chemical Society and National conference on Molecules to Materials (MTM), Ravenshaw University, Cuttack, 4-6 January 2024	en_US
dc.identifier.uri	http://hdl.handle.net/2080/4386	-
dc.description	Copyright belongs to proceeding publisher	en_US
dc.description.abstract	A Pd(II)-catalyzed dehydrogenative remote C4–H coupling of indoles with unfunctionalized arenes at room temperature was reported. The weak chelating trifluoroacetyl group at C3-position was served as a directing group for the remote C4-H activation. Arenes with a wide range of substituents were employed as the coupling partner in the dehydrogenative cross-coupling reaction.	en_US
dc.subject	Indoles	en_US
dc.subject	Trifluoroacetyl group	en_US
dc.subject	Arenes	en_US
dc.title	Weak Chelating Group Directed Palladium-catalyzed C-4 Arylation of Indoles	en_US
dc.type	Article	en_US
Appears in Collections:	Conference Papers

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