
Please use this identifier to cite or link to this item:
http://hdl.handle.net/123456789/3035
Title: | Ruthenium-Catalyzed Hydroarylation of Anilides with Alkynes: An Efficient Route to Ortho-Alkenylated Anilines |
Authors: | Manikandan, R. Jeganmohan, M. |
Keywords: | Hydrocarbons Chemical reactions Aromatic compounds Organic compounds Arylation |
Issue Date: | 2014 |
Publisher: | American Chemical Society. |
Citation: | Organic Letters, 16(3), pp.912-915. |
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. |
URI: | https://pubs.acs.org/doi/10.1021/ol403666s http://hdl.handle.net/123456789/3035 |
Appears in Collections: | Research Articles |
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