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dc.contributor.authorGómez, Ana M.-
dc.contributor.authorBarrio, Aitor-
dc.contributor.authorPedregosa, Ana-
dc.contributor.authorUriel, Clara-
dc.contributor.authorValverde, Serafín-
dc.contributor.authorLópez, J. Cristobal-
dc.date.accessioned2013-11-06T12:15:35Z-
dc.date.available2013-11-06T12:15:35Z-
dc.date.issued2010-
dc.identifierdoi: 10.1002/ejoc.201000170-
dc.identifierissn: 1434-193X-
dc.identifiere-issn: 1099-0690-
dc.identifier.citationEuropean Journal of Organic Chemistry: 2910- 2920 (2010)-
dc.identifier.urihttp://hdl.handle.net/10261/85673-
dc.description.abstractFuranose- and pyranose-derived mono- and dihalo-exo-glycals undergo Sonogashira coupling reactions in the presence of Pd catalysts to give carbohydrate-derived enynes in a completely stereoselective manner. On the other hand, a furanose-derived 2, 3-anhydrohalo-exo-glycal, available from D-mannose in five steps, undergoes Pd0-catalyzed Sonogashira coupling, leading to 2-deoxyenynes. © 2010 Wiley-VCH Verlag GmbH & Co. KGaA,.-
dc.language.isoeng-
dc.publisherJohn Wiley & Sons-
dc.rightsclosedAccess-
dc.titleSonogashira couplings of halo- and epoxy-halo-exo-glycals: Concise entry to carbohydrate-derived enynes-
dc.typeartículo-
dc.identifier.doi10.1002/ejoc.201000170-
dc.date.updated2013-11-06T12:15:35Z-
dc.description.versionPeer Reviewed-
Appears in Collections:(IQOG) Artículos
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