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dc.contributor.authorDorta, Rosa L.en_US
dc.contributor.authorRodríguez Morales, María S.en_US
dc.contributor.authorSalazar, José A.en_US
dc.contributor.authorSuárez, Ernesto-
dc.date.accessioned2009-09-29T07:55:43Z-
dc.date.available2009-09-29T07:55:43Z-
dc.date.issued1997-06-30en_US
dc.identifier.citationTetrahedron Letters 38(26): 4675-4678 (1997)en_US
dc.identifier.issn0040-4039-
dc.identifier.urihttp://hdl.handle.net/10261/17250-
dc.description4 pages, 1 table, 2 schemes.-
dc.description.abstractThe reduction of optically active 2,3-epoxy alcohols, suitably prepared by the Sharpless asymmetric epoxidation of primary allylic alcohols, with the system triphenylphosphine/iodine/imidazole/2,6-lutidine/water, leads in a single step to optically active secondary and tertiary allylic alcohols.-
dc.description.sponsorshipThis work was supported by the Investigation Programme no. PB93-0171 of the Dirección General de Investigación Científica y Técnica.-
dc.format.extent2373 bytes-
dc.format.extent314136 bytes-
dc.format.mimetypetext/plain-
dc.format.mimetypeapplication/pdf-
dc.language.isoengen_US
dc.publisherElsevier-
dc.rightsclosedAccessen_US
dc.title1,3-Transposition of primary allylic alcohols: Synthesis of optically active secondary and tertiary allylic alcoholsen_US
dc.typeartículoen_US
dc.identifier.doi10.1016/S0040-4039(97)00964-7-
dc.relation.publisherversionhttp://dx.doi.org/10.1016/S0040-4039(97)00964-7-
dc.contributor.funderDirección General de Investigación Científica y Técnica, DGICT (España)-
dc.identifier.funderhttp://dx.doi.org/10.13039/501100008737es_ES
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