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dc.contributor.authorVillorbina Noguera, Gemma
dc.contributor.authorTomàs, Albert
dc.contributor.authorEscribà i Gelonch, Marc
dc.contributor.authorOromí Farrús, Mireia
dc.contributor.authorEras i Joli, Jordi
dc.contributor.authorBalcells Fluvià, Mercè
dc.contributor.authorCanela i Garayoa, Ramon
dc.date.accessioned2016-11-03T12:52:35Z
dc.date.issued2009
dc.identifier.issn0040-4039
dc.identifier.urihttp://hdl.handle.net/10459.1/58371
dc.description.abstractWe describe here the first example in which glycerol has been transformed into chlorohydrin esters using an ionic liquid and hydrated aluminium chloride. The method avoids using Crown-18 ether, which was needed to obtain a similar yield when KCl was used. Alkyl and aryl acids can be used, although yields are very dependent on the carboxylic acid used.ca_ES
dc.description.sponsorshipThis work was supported by a Grant-in-Aid from the Secretaría de Estado de Política Científica y Tecnológica of the Spanish Ministry of Education and Culture (contract Grant No.: CTQ2006-07451/PPQ).ca_ES
dc.language.isoengca_ES
dc.publisherElsevierca_ES
dc.relationMIECI/PN2004-2007/CTQ2006-07451/PPQca_ES
dc.relation.isformatofReproducció del document publicat a https://doi.org/10.1016/j.tetlet.2009.03.183ca_ES
dc.relation.ispartofTetrahedron Letters, 2009, vol. 50, núm. 23, p. 2828–2830ca_ES
dc.rights(c) Elsevier, 2009ca_ES
dc.subject[BMIM][PF6]ca_ES
dc.subjectChlorohydrin estersca_ES
dc.subjectGlycerolca_ES
dc.subjectHydrated aluminium chlorideca_ES
dc.subjectIonic liquidca_ES
dc.subjectSubstitutionca_ES
dc.titleCombining AlCl3·6H2O and an ionic liquid to prepare chlorohydrin esters from glycerolca_ES
dc.typearticleca_ES
dc.identifier.idgrec013887
dc.type.versionpublishedVersionca_ES
dc.rights.accessRightsinfo:eu-repo/semantics/restrictedAccessca_ES
dc.identifier.doihttps://doi.org/10.1016/j.tetlet.2009.03.183
dc.date.embargoEndDate10000-01-01


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