Please use this identifier to cite or link to this item:
http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1961
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Padala, Kishor | en_US |
dc.contributor.author | JEGANMOHAN, MASILAMANI | en_US |
dc.date.accessioned | 2019-02-25T09:02:09Z | |
dc.date.available | 2019-02-25T09:02:09Z | |
dc.date.issued | 2014-04 | en_US |
dc.identifier.citation | Chemistry - A European Journal, 20(14), 4092-4097. | en_US |
dc.identifier.issn | 0947-6539 | en_US |
dc.identifier.issn | 1521-3765 | en_US |
dc.identifier.uri | http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1961 | - |
dc.identifier.uri | https://doi.org/10.1002/chem.201304646 | en_US |
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 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.iso | en | en_US |
dc.publisher | Wiley | en_US |
dc.subject | Ortho?Benzoxylation | en_US |
dc.subject | N?Alkyl Benzamides | en_US |
dc.subject | Aromatic Acids Catalyzed | en_US |
dc.subject | Optimized reaction conditions | en_US |
dc.subject | 2014 | 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 |
dc.contributor.department | Dept. of Chemistry | en_US |
dc.identifier.sourcetitle | Chemistry - A European Journal | en_US |
dc.publication.originofpublisher | Foreign | en_US |
Appears in Collections: | JOURNAL ARTICLES |
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.