Ruthenium-Catalyzed Hydroarylation of Anilides with Alkynes: An Efficient Route to Ortho-Alkenylated Anilines

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