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Cp2TiCl-catalyzed highly stereoselective intramolecular epoxide allylation using allyl carbonates

dc.contributor.authorRodríguez Márquez, Irenees_ES
dc.contributor.authorMilán Delgado, Albaes_ES
dc.contributor.authorGonzález Campaña, Araceli es_ES
dc.contributor.authorCuerva Carvajal, Juan Manuel es_ES
dc.date.accessioned2017-07-28T10:19:05Z
dc.date.available2017-07-28T10:19:05Z
dc.date.issued2014-01-14
dc.identifier.citationRodríguez Márquez, I.; et al. Cp2TiCl-catalyzed highly stereoselective intramolecular epoxide allylation using allyl carbonates. Organic Chemistry Frontiers, 4: 373-381 (2014). [http://hdl.handle.net/10481/47294]es_ES
dc.identifier.issn2052-4129
dc.identifier.issn2052-4110
dc.identifier.urihttp://hdl.handle.net/10481/47294
dc.description.abstractA useful method for the diastereoselective synthesis of vinyl substituted carbo- and heterocycles is described. Highly functionalized structures difficult to achieve by other methodologies are obtained in a single step by this procedure.en_EN
dc.description.sponsorshipThis research was funded by the Ministerio de Ciencia e Innovación (Spain) (project CTQ-2011.22455). I.R.M. thanks the MEC (Spain) for a predoctoral FPU fellowship. A.M. thanks the University of Granada for a postdoctoral contract (‘Contrato Puente’). A.G.C. thanks the MICINN (Spain) for a postdoctoral contract ‘Juan de la Cierva’ and University of Granada.en_EN
dc.language.isoenges_ES
dc.publisherRoyal Society of Chemistryes_ES
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivs 3.0 Licensees_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es_ES
dc.subjectIntramolecular epoxide allylationen_EN
dc.subjectAllyl carbonatesen_EN
dc.subjectDiastereoselective synthesisen_EN
dc.titleCp2TiCl-catalyzed highly stereoselective intramolecular epoxide allylation using allyl carbonatesen_EN
dc.typeinfo:eu-repo/semantics/articleen_EN
dc.rights.accessRightsinfo:eu-repo/semantics/openAccessen_EN
dc.identifier.doi10.1039/C4QO00012A


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