Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1648
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dc.contributor.authorREDDY, MALLU CHENNAen_US
dc.contributor.authorJEGANMOHAN, MASILAMANIen_US
dc.date.accessioned2019-02-14T05:02:00Z
dc.date.available2019-02-14T05:02:00Z
dc.date.issued2012-11en_US
dc.identifier.citationChemical Communications, 49(5), 481-483.en_US
dc.identifier.issn1359-7345en_US
dc.identifier.issn1364-548Xen_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1648-
dc.identifier.urihttps://doi.org/10.1039/C2CC37758Fen_US
dc.description.abstractChelation-assisted alkenylation of ortho C-H bond of aryl carbamates with alkynes in the presence of a ruthenium catalyst, AgSbF6 and pivalic acid gives highly substituted alkene derivatives in good to excellent yields in a highly regio- and stereoselective manner.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectstereoselective hydroarylationen_US
dc.subjectCarbamatesen_US
dc.subjectAlkynes via C-H bond activationen_US
dc.subjectStereoisomericen_US
dc.subjectStereoselective manneren_US
dc.subject2012en_US
dc.titleRuthenium-catalyzed highly regio- and stereoselective hydroarylation of aryl carbamates with alkynes via C-H bond activationen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleChemical Communicationsen_US
dc.publication.originofpublisherForeignen_US
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