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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Manikandan, Rajendran | 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 | 2014-02 | en_US |
dc.identifier.citation | Organic Letters, 16(3),912-915. | en_US |
dc.identifier.issn | 1523-7060 | en_US |
dc.identifier.issn | 1523-7052 | en_US |
dc.identifier.uri | http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1960 | - |
dc.identifier.uri | https://doi.org/10.1021/ol403666s | en_US |
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 | Ruthenium-Catalyzed Hydroarylation | en_US |
dc.subject | Anilides with Alkynes | en_US |
dc.subject | Ortho-Alkenylated Anilines | en_US |
dc.subject | Presence of HCl | en_US |
dc.subject | 2014 | 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 |
dc.contributor.department | Dept. of Chemistry | en_US |
dc.identifier.sourcetitle | Organic Letters | en_US |
dc.publication.originofpublisher | Foreign | en_US |
Appears in Collections: | JOURNAL ARTICLES |
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