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dc.contributor.authorChiara, José Luis-
dc.contributor.authorValle, Nuria-
dc.date.accessioned2011-01-04T14:08:28Z-
dc.date.available2011-01-04T14:08:28Z-
dc.date.issued1995-08-
dc.identifier.citationTetrahedron Asymmetry 6(8): 1895-1898 (1995)es_ES
dc.identifier.issn0957-4166-
dc.identifier.urihttp://hdl.handle.net/10261/30919-
dc.description4 páginas, 1 figura.es_ES
dc.description.abstractA synthesis of L-chiro-inositol and (−)-conduritol F starting from readily available D -sorbitol is described. The route involves as a key step an efficient one-pot sequence consisting of the Swern oxidation of a 1,6-diol followed by a highly stereoselective intramolecular pinacol coupling of the resultant dialdehyde, promoted by samarium diiodide.es_ES
dc.description.sponsorshipThis work was supported by MEC-DGICYT (Grant PB93-0127-C02-01).es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.rightsclosedAccesses_ES
dc.titleSynthesis of L-chiro-inositol and (−)-conduritol F from D -sorbitol by a highly stereoselective intramolecular pinacol coupling promoted by samarium diiodidees_ES
dc.typeartículoes_ES
dc.identifier.doi10.1016/0957-4166(95)00246-L-
dc.description.peerreviewedPeer reviewedes_ES
dc.relation.publisherversionhttp://dx.doi.org/10.1016/0957-4166(95)00246-Les_ES
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