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Ruthenium-catalyzed intramolecular selective halogenation of O-methylbenzohydroximoyl halides: a new route to halogenated aromatic nitriles

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dc.contributor.author Chinnagolla, Ravi Kiran en_US
dc.contributor.author Pimparkar, Sandeep en_US
dc.contributor.author JEGANMOHAN, MASILAMANI en_US
dc.date.accessioned 2019-02-14T05:02:00Z
dc.date.available 2019-02-14T05:02:00Z
dc.date.issued 2013-02 en_US
dc.identifier.citation Chemical Communications, 49(54), 3146-3148. en_US
dc.identifier.issn 1359-7345 en_US
dc.identifier.issn 1364-548X en_US
dc.identifier.uri http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1647
dc.identifier.uri https://doi.org/10.1039/C3CC41124A en_US
dc.description.abstract The 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.iso en en_US
dc.publisher Royal Society of Chemistry en_US
dc.subject Ruthenium-catalyzed en_US
dc.subject Oxidative cyclization en_US
dc.subject Aromatic and heteroaromatic en_US
dc.subject Route to isoquinolones en_US
dc.subject Halogenated aromatic nitriles en_US
dc.subject Intramolecular halogenation en_US
dc.subject N-methoxybenzimidoyl en_US
dc.subject 2013 en_US
dc.title Ruthenium-catalyzed intramolecular selective halogenation of O-methylbenzohydroximoyl halides: a new route to halogenated aromatic nitriles en_US
dc.type Article en_US
dc.contributor.department Dept. of Chemistry en_US
dc.identifier.sourcetitle Chemical Communications en_US
dc.publication.originofpublisher Foreign en_US


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