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dc.contributor.authorCHAUDHARI, MORESHWAR B.en_US
dc.contributor.authorBISHT, GIRISH SINGHen_US
dc.contributor.authorKUMARI, POOJAen_US
dc.contributor.authorGNANAPRAKASAM, BOOPATHYen_US
dc.date.accessioned2019-04-26T09:12:30Z
dc.date.available2019-04-26T09:12:30Z
dc.date.issued2016-09en_US
dc.identifier.citationOrganic and Biomolecular Chemistry, 14(39), 9215-9220.en_US
dc.identifier.issn1477-0520en_US
dc.identifier.issn1477-0539en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2498-
dc.identifier.urihttps://doi.org/10.1039/C6OB01786Jen_US
dc.description.abstractThe highly efficient direct α-alkylation of unactivated amides has been accomplished using alcohols in the presence of the Ru-PNN catalyst (0.1 mol%) with a high turnover number. Using this approach, 2-oxindole was directly transformed into C3-alkylated 3-hydroxyindolin-2-one in one step without the use of any oxidant.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectRuthenium-catalyzeden_US
dc.subjectDirect ?-alkylationen_US
dc.subjectPharmaceutical compoundsen_US
dc.subjectRu-PNN catalysten_US
dc.subjectNMR and mass analysisen_US
dc.subject2016en_US
dc.titleRuthenium-catalyzed direct α-alkylation of amides using alcoholsen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleOrganic and Biomolecular Chemistryen_US
dc.publication.originofpublisherForeignen_US
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