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Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2509
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dc.contributor.authorManoharan, Ramasamyen_US
dc.contributor.authorSivakumar, Ganesanen_US
dc.contributor.authorJAYAKANNAN, MANICKAMen_US
dc.date.accessioned2019-04-26T09:13:53Z
dc.date.available2019-04-26T09:13:53Z
dc.date.issued2016-07en_US
dc.identifier.citationChemical Communications, 52(69), 10533-10536.en_US
dc.identifier.issn1359-7345en_US
dc.identifier.issn1364-548Xen_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2509-
dc.identifier.urihttps://doi.org/10.1039/C6CC04835Hen_US
dc.description.abstractA cobalt-catalyzed C–H olefination of aromatic and heteroaromatic amides with unactivated alkenes, allyl acetates and allyl alcohols is described. This method offers an efficient route for the synthesis of vinyl and allyl benzamides in a highly stereoselective manner. It is observed that the ortho substituent on the benzamide moiety is crucial for the observation of allylated products in unactivated alkenes.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectC-H bond functionalizationen_US
dc.subjectCobalt-catalyzed C-H olefinationen_US
dc.subjectUnactivated alkenesen_US
dc.subjectHighly regioselective manneren_US
dc.subject2016en_US
dc.titleCobalt-catalyzed C-H olefination of aromatics with unactivated alkenesen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleChemical Communicationsen_US
dc.publication.originofpublisherForeignen_US
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