Pd(II)-Catalyzed Direct β-Arylation of C(sp3)-H Bonds of Aliphatic and Alicyclic Carboxamides Via One-pot Method

Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/610

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DC Field	Value	Language
dc.contributor.author	Mohan, Sruthi	-
dc.date.accessioned	2016-09-06T15:25:32Z	-
dc.date.available	2016-09-06T15:25:32Z	-
dc.date.issued	2016-09-03	-
dc.identifier.uri	http://hdl.handle.net/123456789/610	-
dc.description.abstract	A step economical one-pot multicomponent reaction protocol comprising the installation of the bidentate directing group followed by the Pd(II)-catalyzed C-H activation and β-arylation of C(sp3)-H bonds of carboxamides is reported. Accordingly, the reaction of a mixture of an acid chloride, bidentate ligand (e.g., 8-aminoquinoline), and an aryl iodide in the presence of the Pd(OAc)2 catalyst and Ag2CO3 additive directly afforded the corresponding β-C-H -arylated N-(quinolin-8-yl) carboxamide derivatives.	en_US
dc.description.sponsorship	IISER-M	en_US
dc.language.iso	en	en_US
dc.publisher	IISER-M	en_US
dc.subject	Chemistry	en_US
dc.subject	Alicyclic Carboxamides	en_US
dc.subject	Aliphatic Carboxamides	en_US
dc.title	Pd(II)-Catalyzed Direct β-Arylation of C(sp3)-H Bonds of Aliphatic and Alicyclic Carboxamides Via One-pot Method	en_US
dc.type	Thesis	en_US
Appears in Collections:	MS-11

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