Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1961
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dc.contributor.authorPadala, Kishoren_US
dc.contributor.authorJEGANMOHAN, MASILAMANIen_US
dc.date.accessioned2019-02-25T09:02:09Z
dc.date.available2019-02-25T09:02:09Z
dc.date.issued2014-04en_US
dc.identifier.citationChemistry - A European Journal, 20(14), 4092-4097.en_US
dc.identifier.issn0947-6539en_US
dc.identifier.issn1521-3765en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1961-
dc.identifier.urihttps://doi.org/10.1002/chem.201304646en_US
dc.description.abstractA highly regioselective ortho‐benzoxylation of N‐alkyl benzamides with aromatic acids in the presence of [{RuCl2(p‐cymene)}2], AgSbF6, and (NH4)2S2O8 in 1,2‐dichloroethane at 100 °C for 24 h affording ortho‐benzoxylated N‐alkyl benzamides by C-H bond activation is described. Further, Ru‐catalyzed alkenylation is done at the ortho C-H bond of benzoxylated N‐alkyl benzamides with alkenes in water solvent. Subsequently, the benzoxyl moiety of N‐alkyl benzamides was converted into a hydroxyl group in the presence of base or acid. A possible reaction mechanism was proposed to account for the present coupling reaction.en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.subjectOrtho?Benzoxylationen_US
dc.subjectN?Alkyl Benzamidesen_US
dc.subjectAromatic Acids Catalyzeden_US
dc.subjectOptimized reaction conditionsen_US
dc.subject2014en_US
dc.titleortho‐Benzoxylation of N‐Alkyl Benzamides with Aromatic Acids Catalyzed by Ruthenium(II) Complexen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleChemistry - A European Journalen_US
dc.publication.originofpublisherForeignen_US
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