Palladium-Catalyzed Tandem Intramolecular Oxy/Amino-Palladation/Isocyanide Insertion: Synthesis of α-Benzofuranyl/Indolylacetamides

Thirupathi, Nuligonda; Babu, M H; Dwivedi, Vikas; Reddy, M S

dc.contributor.author	Thirupathi, Nuligonda
dc.contributor.author	Babu, M H
dc.contributor.author	Dwivedi, Vikas
dc.contributor.author	Reddy, M S
dc.date.accessioned	2014-08-28T11:37:32Z
dc.date.available	2014-08-28T11:37:32Z
dc.date.issued	2014
dc.identifier.citation	Organic Letters, 2014, 16 (11), 2908–2911	en
dc.identifier.uri	http://hdl.handle.net/123456789/1381
dc.description.abstract	Anovel palladium-catalyzed approach to 2-benzofuranyl/indolylacetamides from 1-(o-hydroxy/aminophenyl)propargylic alcohols and isocyanides is described. The reaction proceeds through a cascade that includes oxy/amino-palladation, isocyanide insertion and 1,4-hydroxyl migration. No oxidant or ligand is needed to promote the cascade and the reactions are carried out in mild conditions to afford the products through high functional tolerance.	en
dc.format.extent	419923 bytes
dc.format.mimetype	application/pdf
dc.language.iso	en	en
dc.relation.ispartofseries	CSIR-CDRI Communication No. 8688	en
dc.subject	Palladium-Catalyzed	en
dc.subject	Tandem Intramolecular	en
dc.subject	Oxy/Amino-Palladation/Isocyanide	en
dc.subject	Insertion: Synthesis	en
dc.title	Palladium-Catalyzed Tandem Intramolecular Oxy/Amino-Palladation/Isocyanide Insertion: Synthesis of α-Benzofuranyl/Indolylacetamides	en
dc.type	Article	en