Highly Regio- And Stereoselective Heck Reaction Of Allylic Esters With Arenediazonium Salts: Application To The Synthesis Of Kavalactones

dc.creatorMoro A.V.
dc.creatorCardoso F.S.P.
dc.creatorCorreia C.R.D.
dc.date2009
dc.date2015-06-26T13:38:17Z
dc.date2015-11-26T15:40:04Z
dc.date2015-06-26T13:38:17Z
dc.date2015-11-26T15:40:04Z
dc.date.accessioned2018-03-28T22:48:34Z
dc.date.available2018-03-28T22:48:34Z
dc.identifier
dc.identifierOrganic Letters. , v. 11, n. 16, p. 3642 - 3645, 2009.
dc.identifier15237060
dc.identifier10.1021/ol901416e
dc.identifierhttp://www.scopus.com/inward/record.url?eid=2-s2.0-68949132409&partnerID=40&md5=372a6869f62d53d11eee3847ceba603a
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/93007
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/93007
dc.identifier2-s2.0-68949132409
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1264290
dc.descriptionImage Presented A highly efficient palladium-catalyzed Heck reaction of allylic esters with arenediazonium salts is described. The reaction proceeds under mild conditions, with excellent to total regio- and stereochemical control and with retention of the traditional leaving group. Furthermore, the generality of the present methodology is illustrated by the short total synthesis of the natural kavalactones, yangonine, (±)-methysticin, and (±)-dihydromethysticin. © 2009 American Chemical Society.
dc.description11
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dc.languageen
dc.publisher
dc.relationOrganic Letters
dc.rightsfechado
dc.sourceScopus
dc.titleHighly Regio- And Stereoselective Heck Reaction Of Allylic Esters With Arenediazonium Salts: Application To The Synthesis Of Kavalactones
dc.typeArtículos de revistas


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