Synthetic tools for the characterization of galactofuranosyl transferases. Glycosylations via acylated glycosyl iodides | ||
| dc.conicet.organizacion | Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Centro de Investigaciones en Hidratos de Carbono | |
| dc.conicet.organizacion | Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Centro de Investigaciones en Hidratos de Carbono | |
| dc.conicet.paisOrganizacion | Argentina | |
| dc.conicet.paisOrganizacion | Argentina | |
| dc.conicet.produccionid | 2992242 | |
| dc.contributor.author | Baldoni, Luciana | |
| dc.contributor.author | Marino, María Carla | |
| dc.date.accessioned | 2015-09-24T19:36:40Z | |
| dc.date.available | 2015-09-24T19:36:40Z | |
| dc.date.issued | 2013-06-07 | |
| dc.date.updated | 2016-03-30 10:35:44.97925-03 | |
| dc.description.abstract | With the aim to develop synthetic tools for the characterization of galactofuranosyltransferases, the synthesis of 9-decenyl glycosides of D-Manp, D-Galf and beta-D-Galf-(1,3)-D-Manp was targeted. The interest in the alkenyl aglycone arises from its potential conjugation reactions, once the terminal double bond has been conveniently functionalized. The glycosylation of beta-D-Galf-(1,3)-D-Manp was attempted by two different approaches: the trichloroacetimidate method and the glycosylation via the glycosyl iodide. The conditions for the latter were established on the basis of glycosylation assays of per-Oacetylmannose.On the other hand, the study of glycosylation reactions via per-O-bezoylated galactofuranosyl iodide confirms the versatility of glycosyl iodides as donors. | es |
| dc.description.fil | Fil: Baldoni, Luciana. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Centro de Investigaciones en Hidratos de Carbono; Argentina | |
| dc.description.fil | Fil: Marino, María Carla. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Centro de Investigaciones en Hidratos de Carbono; Argentina | |
| dc.format | application/pdf | es |
| dc.identifier.citation | Baldoni, Luciana; Marino, María Carla; Synthetic tools for the characterization of galactofuranosyl transferases. Glycosylations via acylated glycosyl iodides; Elsevier; Carbohydrate Research; 374; 7-6-2013; 75-81 | es |
| dc.identifier.issn | 0008-6215 | es |
| dc.identifier.uri | http://hdl.handle.net/11336/2105 | |
| dc.journal.ciudad | Amsterdam | es |
| dc.journal.pagination | 75-81 | es |
| dc.journal.pais | Países Bajos | es |
| dc.journal.title | Carbohydrate Research | es |
| dc.journal.volume | 374 | es |
| dc.language.iso | eng | es |
| dc.publisher | Elsevier | es |
| dc.relation.alternativeid | info:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S0008621513001286 | |
| dc.relation.alternativeid | info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.carres.2013.03.032 | |
| dc.rights | info:eu-repo/semantics/openAccess | * |
| dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/2.5/ar/ | * |
| dc.subject | Galactofuranosyl Iodides | es |
| dc.subject | Mannopyranosyl Iodide | es |
| dc.subject | Per-O-Benzoylated-Galactofuranosyl Iodide | es |
| dc.subject | Per-O-Tert-Butyldimethylsilyl-B-D | es |
| dc.subject | Galactofuranose | es |
| dc.subject | Galactofuranosyl Transferases | es |
| dc.subject.classification | Química Orgánica | es |
| dc.subject.classification | Ciencias Químicas | es |
| dc.subject.classification | CIENCIAS NATURALES Y EXACTAS | es |
| dc.title | Synthetic tools for the characterization of galactofuranosyl transferases. Glycosylations via acylated glycosyl iodides | es |
| dc.type | info:eu-repo/semantics/article | |
| dc.type | info:ar-repo/semantics/artículo | |
| dc.type | info:eu-repo/semantics/publishedVersion | |
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