The First Examples Of The Enantioselective Heck-matsuda Reaction: Arylation Of Unactivated Cyclic Olefins Using Chiral Bisoxazolines

dc.creatorCorreia C.R.D.
dc.creatorOliveira C.C.
dc.creatorSalles Jr. A.G.
dc.creatorSantos E.A.F.
dc.date2012
dc.date2015-06-26T20:28:22Z
dc.date2015-11-26T14:24:23Z
dc.date2015-06-26T20:28:22Z
dc.date2015-11-26T14:24:23Z
dc.date.accessioned2018-03-28T21:26:33Z
dc.date.available2018-03-28T21:26:33Z
dc.identifier
dc.identifierTetrahedron Letters. , v. 53, n. 26, p. 3325 - 3328, 2012.
dc.identifier404039
dc.identifier10.1016/j.tetlet.2012.04.079
dc.identifierhttp://www.scopus.com/inward/record.url?eid=2-s2.0-84861528561&partnerID=40&md5=ab15fc4b3a6b1ec4c419f81debe34676
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/96645
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/96645
dc.identifier2-s2.0-84861528561
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1245388
dc.descriptionSuccessful enantioselective Heck-Matsuda arylations were accomplished for the first time using chiral bisoxazolines as ligands. Enantioselective Heck arylations were performed with several cyclic nonactivated olefins to provide the Heck products in 63-96% isolated yields and in enantiomeric excesses of 54% up to 84%. © 2012 Elsevier Ltd. All rights reserved.
dc.description53
dc.description26
dc.description3325
dc.description3328
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dc.languageen
dc.publisher
dc.relationTetrahedron Letters
dc.rightsfechado
dc.sourceScopus
dc.titleThe First Examples Of The Enantioselective Heck-matsuda Reaction: Arylation Of Unactivated Cyclic Olefins Using Chiral Bisoxazolines
dc.typeArtículos de revistas


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