Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1650
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dc.contributor.authorChinnagolla, Ravi Kiranen_US
dc.contributor.authorPimparkar, Sandeepen_US
dc.contributor.authorJEGANMOHAN, MASILAMANIen_US
dc.date.accessioned2019-02-14T05:02:00Z-
dc.date.available2019-02-14T05:02:00Z-
dc.date.issued2013-03en_US
dc.identifier.citationChemical Communications, 49(35),3703-3705.en_US
dc.identifier.issn1359-7345en_US
dc.identifier.issn1364-548Xen_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1650-
dc.identifier.urihttps://doi.org/10.1039/C3CC41269Een_US
dc.description.abstractA ruthenium-catalyzed highly regioselective cyclization of substituted N-methoxy benzimidoyl halides with alkynes in the presence of CsOAc (25 mol%) to give substituted 1-halo and 1-alkoxy substituted isoquinolines in good to excellent yields is described.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectRegioselective synthesisen_US
dc.subjectO-methylbenzohydroximoylen_US
dc.subjectN-methoxybenzimidoyl chlorideen_US
dc.subjectCarbonen_US
dc.subjectOptimization studiesen_US
dc.subject2013en_US
dc.titleA regioselective synthesis of 1-haloisoquinolines via ruthenium-catalyzed cyclization of O-methylbenzohydroximoyl halides with alkynesen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleChemical Communicationsen_US
dc.publication.originofpublisherForeignen_US
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