
Please use this identifier to cite or link to this item:
http://hdl.handle.net/123456789/2979
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DC Field | Value | Language |
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dc.contributor.author | Padala, K. | - |
dc.contributor.author | Jeganmohan, M. | - |
dc.date.accessioned | 2020-12-10T10:46:48Z | - |
dc.date.available | 2020-12-10T10:46:48Z | - |
dc.date.issued | 2014 | - |
dc.identifier.citation | Chemistry - A European Journal,20(14), pp.4092-4097. | en_US |
dc.identifier.other | https://doi.org/10.1002/chem.201304646 | - |
dc.identifier.uri | https://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/chem.201304646 | - |
dc.identifier.uri | http://hdl.handle.net/123456789/2979 | - |
dc.description.abstract | A 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 CH bond activation is described. Further, Ru‐catalyzed alkenylation is done at the ortho CH 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.iso | en | en_US |
dc.publisher | Wiley-VCH Verlag | en_US |
dc.subject | Ortho‐Benzoxylation | en_US |
dc.subject | N‐Alkyl Benzamides | en_US |
dc.subject | Aromatic Acids | en_US |
dc.title | Ortho‐Benzoxylation of N‐Alkyl Benzamides with Aromatic Acids Catalyzed by Ruthenium(II) Complex | en_US |
dc.type | Article | en_US |
Appears in Collections: | Research Articles |
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