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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.issued2013-02en_US
dc.identifier.citationChemical Communications, 49(54), 3146-3148.en_US
dc.identifier.issn1359-7345en_US
dc.identifier.issn1364-548Xen_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1647-
dc.identifier.urihttps://doi.org/10.1039/C3CC41124Aen_US
dc.description.abstractThe intramolecular halogenation of O-methylbenzohydroximoyl halides in the presence of a Ru catalyst and the ligand diphenylacetylene afforded halo substituted aromatic nitriles in a highly regioselective manner. Further, substituted nitriles were converted into substituted tetrazole derivatives in the presence of NaN3 and I2.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.subjectHalogenated aromatic nitrilesen_US
dc.subjectIntramolecular halogenationen_US
dc.subjectN-methoxybenzimidoylen_US
dc.subject2013en_US
dc.titleRuthenium-catalyzed intramolecular selective halogenation of O-methylbenzohydroximoyl halides: a new route to halogenated aromatic nitrilesen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleChemical Communicationsen_US
dc.publication.originofpublisherForeignen_US
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