
Please use this identifier to cite or link to this item:
http://hdl.handle.net/123456789/3035
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DC Field | Value | Language |
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dc.contributor.author | Manikandan, R. | - |
dc.contributor.author | Jeganmohan, M. | - |
dc.date.accessioned | 2020-12-11T06:42:33Z | - |
dc.date.available | 2020-12-11T06:42:33Z | - |
dc.date.issued | 2014 | - |
dc.identifier.citation | Organic Letters, 16(3), pp.912-915. | en_US |
dc.identifier.other | https://doi.org/10.1021/ol403666s | - |
dc.identifier.uri | https://pubs.acs.org/doi/10.1021/ol403666s | - |
dc.identifier.uri | http://hdl.handle.net/123456789/3035 | - |
dc.description.abstract | Acetanilides reacted with symmetrical as well as unsymmetrical alkynes in the presence of [{RuCl2(p-cymene)}2], pivalic acid, and AgSbF6 in iso-PrOH providing ortho-alkenylated acetanilides in a highly regio- and stereoselective manner. Later, ortho-alkenylated acetanilides were converted into ortho-alkenylated anilines in the presence of HCl. | en_US |
dc.language.iso | en | en_US |
dc.publisher | American Chemical Society. | en_US |
dc.subject | Hydrocarbons | en_US |
dc.subject | Chemical reactions | en_US |
dc.subject | Aromatic compounds | en_US |
dc.subject | Organic compounds | en_US |
dc.subject | Arylation | en_US |
dc.title | Ruthenium-Catalyzed Hydroarylation of Anilides with Alkynes: An Efficient Route to Ortho-Alkenylated Anilines | en_US |
dc.type | Article | en_US |
Appears in Collections: | Research Articles |
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