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dc.contributor.authorFrancisco, Cosme G.en_US
dc.contributor.authorGonzález Martín, Concepción C.en_US
dc.contributor.authorSuárez, Ernestoen_US
dc.date.accessioned2009-09-29T07:54:41Z-
dc.date.available2009-09-29T07:54:41Z-
dc.date.issued1996-03-04en_US
dc.identifier.citationTetrahedron Letters 37(10): 1687-1690 (1996)en_US
dc.identifier.issn0040-4039-
dc.identifier.urihttp://hdl.handle.net/10261/17247-
dc.description4 pages, 1 table, 1 scheme.-
dc.description.abstractAldopyranosuronic and aldofuranosuronic acid lactones, with one carbon less, can be specifically obtained when hexuronic and penturonic acids in pyranose or furanose forms undergo a tandem β-fragmentation-cyclization reaction promoted by the system (diacetoxyiodo)benzene-iodine, under mild conditions. The lactones are formed via 1,5 and 1,6 intramolecular cyclization.-
dc.description.sponsorshipThis work was supported by the Investigation Programme n° PB93-0171 of the Dirección General de Investigación Científica y Técnica and Programmes n° 93/030 and 93/014 of the Dirección General de Universidades e Investigación del Gobiemo de Canarias. C.C.G. thanks the Dirección General de Universidades e Investigación del Gobierno de Canarias for a fellowship.-
dc.format.extent2373 bytes-
dc.format.extent349335 bytes-
dc.format.mimetypetext/plain-
dc.format.mimetypeapplication/pdf-
dc.language.isoengen_US
dc.publisherElsevier-
dc.rightsclosedAccessen_US
dc.titleFragmentation of carbohydrate anomeric alkoxy radicals. A new synthesis of alduronic acid lactonesen_US
dc.typeartículoen_US
dc.identifier.doi10.1016/0040-4039(96)00107-4-
dc.relation.publisherversionhttp://dx.doi.org/10.1016/0040-4039(96)00107-4-
dc.contributor.funderDirección General de Investigación Científica y Técnica, DGICT (España)-
dc.contributor.funderGobierno de Canarias-
dc.identifier.funderhttp://dx.doi.org/10.13039/501100008737es_ES
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