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

dc.contributor.authorManikandan, R.
dc.contributor.authorJeganmohan, M.
dc.date.accessioned2020-12-11T06:42:33Z
dc.date.available2020-12-11T06:42:33Z
dc.date.issued2014
dc.description.abstractAcetanilides 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.identifier.citationOrganic Letters, 16(3), pp.912-915.en_US
dc.identifier.otherhttps://doi.org/10.1021/ol403666s
dc.identifier.urihttps://pubs.acs.org/doi/10.1021/ol403666s
dc.identifier.urihttp://hdl.handle.net/123456789/3035
dc.language.isoenen_US
dc.publisherAmerican Chemical Society.en_US
dc.subjectHydrocarbonsen_US
dc.subjectChemical reactionsen_US
dc.subjectAromatic compoundsen_US
dc.subjectOrganic compoundsen_US
dc.subjectArylationen_US
dc.titleRuthenium-Catalyzed Hydroarylation of Anilides with Alkynes: An Efficient Route to Ortho-Alkenylated Anilinesen_US
dc.typeArticleen_US

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