Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1645
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dc.contributor.authorREDDY, MALLU CHENNAen_US
dc.contributor.authorManikandan, Rajendranen_US
dc.contributor.authorJEGANMOHAN, MASILAMANIen_US
dc.date.accessioned2019-02-14T05:02:00Z
dc.date.available2019-02-14T05:02:00Z
dc.date.issued2013-05en_US
dc.identifier.citationChemical Communications, 49(54), 6060-6062.en_US
dc.identifier.issn1359-7345en_US
dc.identifier.issn1364-548Xen_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1645-
dc.identifier.urihttps://doi.org/10.1039/C3CC42683Aen_US
dc.description.abstractThe oxidative cyclization of aromatic and heteroaromatic nitriles with alkynes in the presence of a catalytic amount of [{RuCl2(p-cymene)}2], Cu(OAc)2-H2O and KPF6 in acetic acid under air gave isoquinolones in good to excellent yields.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectRuthenium-catalyzeden_US
dc.subjectOxidative cyclizationen_US
dc.subjectAromatic and heteroaromaticen_US
dc.subjectRoute to isoquinolonesen_US
dc.subjectIsoquinolone derivativesen_US
dc.subject2013en_US
dc.titleRuthenium-catalyzed aerobic oxidative cyclization of aromatic and heteroaromatic nitriles with alkynes: a new route to isoquinolonesen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleChemical Communicationsen_US
dc.publication.originofpublisherForeignen_US
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