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

dc.contributor.authorMohan, Sruthi
dc.date.accessioned2016-09-03T05:45:48Z
dc.date.available2016-09-03T05:45:48Z
dc.date.issued2016-09-03
dc.description.abstractA 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.sponsorshipIISER-Men_US
dc.guideBabu, S.A.
dc.identifier.urihttp://hdl.handle.net/123456789/603
dc.language.isoenen_US
dc.publisherIISER-Men_US
dc.subjectChemistryen_US
dc.subjectAlicyclic Carboxamidesen_US
dc.subjectAliphatic Carboxamidesen_US
dc.titlePd(II)-Catalyzed Direct β-Arylation of C(sp3)-H Bonds of Aliphatic and Alicyclic Carboxamides Via One-pot Methoden_US
dc.typeThesisen_US

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