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Ruthenium-Catalyzed ortho Alkenylation of Aromatics with Alkenes at Room Temperature with Hydrogen Evolution

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dc.contributor.author Manikandan, Rajendran en_US
dc.contributor.author Madasamy, Padmaja en_US
dc.contributor.author JAYAKANNAN, MANICKAM en_US
dc.date.accessioned 2019-04-29T10:15:50Z
dc.date.available 2019-04-29T10:15:50Z
dc.date.issued 2016-01 en_US
dc.identifier.citation ACS Catalysis, 6 (1), 230-234. en_US
dc.identifier.issn 2155-5435 en_US
dc.identifier.uri http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/2717
dc.identifier.uri https://doi.org/10.1021/acscatal.5b02218 en_US
dc.description.abstract A ruthenium-catalyzed oxidant-free highly regioselective ortho alkenylation of substituted aromatics such as aromatic amides, aromatic ketoximes, and anilides with alkenes in the presence of AgSbF6 and acetic acid in ClCH2CH2Cl at room temperature is described. The alkenylation reaction provides ortho alkenylated aromatics along with evolution of H2 gas. In the reaction, no oxidant was used, and the whole catalytic reaction has occurred without changing the oxidation state of the metal. en_US
dc.language.iso en en_US
dc.publisher American Chemical Society en_US
dc.subject Ruthenium-Catalyzed en_US
dc.subject Alkenylation en_US
dc.subject Room Temperature en_US
dc.subject Hydrogen Evolution en_US
dc.subject Ambient temperature en_US
dc.subject C?H bond activation en_US
dc.subject Hydrogen evolution en_US
dc.subject Oxidant free en_US
dc.subject Ruthenium catalysis en_US
dc.subject 2016 en_US
dc.title Ruthenium-Catalyzed ortho Alkenylation of Aromatics with Alkenes at Room Temperature with Hydrogen Evolution en_US
dc.type Article en_US
dc.contributor.department Dept. of Chemistry en_US
dc.identifier.sourcetitle ACS Catalysis en_US
dc.publication.originofpublisher Foreign en_US


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