Synthesis of D-galactofuranose-containing molecules: design of galactofuranosyl acceptors.

D-Galactofuranose (D-Galf) is present in glycoconjugates of several pathogenic microorganisms but is absent in mammals, so it is a good target for the development of chemotherapeutic agents for the treatment of microbial infections. This fact has increased interest in the synthesis of D-Galf-contain...

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Detalles Bibliográficos
Autor principal: Marino, C.
Otros Autores: Baldoni, L.
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: 2014
Acceso en línea:Registro en Scopus
DOI
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Registro en la Biblioteca Digital
Aporte de:Registro referencial: Solicitar el recurso aquí
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024 7 |2 scopus  |a 2-s2.0-84906892311 
024 7 |2 cas  |a galactose, 26566-61-0, 50855-33-9, 59-23-4 
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100 1 |a Marino, C. 
245 1 0 |a Synthesis of D-galactofuranose-containing molecules: design of galactofuranosyl acceptors. 
260 |c 2014 
270 1 0 |m Marino, C.email: cmarino@qo.fcen.uba.ar 
506 |2 openaire  |e Política editorial 
520 3 |a D-Galactofuranose (D-Galf) is present in glycoconjugates of several pathogenic microorganisms but is absent in mammals, so it is a good target for the development of chemotherapeutic agents for the treatment of microbial infections. This fact has increased interest in the synthesis of D-Galf-containing molecules for corresponding glycobiological studies. The synthesis of oligosaccharides, glycoconjugates, and mimetics of D-Galf requires specific methods for the preparation of galactose derivatives in the furanosic configuration, the synthesis of appropriate acceptors, and efficient glycosylation methods for the construction of α- and β-D-Galf linkages. This review summarizes the different strategies developed for the preparation of partially protected derivatives of D-Galf, suitable as acceptors for the construction of (1→2), (1→3), (1→5), and (1→6) link- ages, and describes recent applications. Copyright © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.  |l eng 
593 |a CIHIDECAR-CONICET-UBA, Departamento de Química Orgánica, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Pabellón II, Ciudad Universitaria, 1428 Buenos Aires (Argentina). 
690 1 0 |a CARBOHYDRATE 
690 1 0 |a GALACTOSE 
690 1 0 |a GLYCOCONJUGATE 
690 1 0 |a POLYSACCHARIDE 
690 1 0 |a CHEMISTRY 
690 1 0 |a DRUG DESIGN 
690 1 0 |a GALACTOFURANOSIDES 
690 1 0 |a GALACTOFURANOSYL ACCEPTORS 
690 1 0 |a GLYCOSYLATION 
690 1 0 |a METHODOLOGY 
690 1 0 |a ORGANIC SYNTHESIS 
690 1 0 |a REVIEW 
690 1 0 |a SYNTHESIS 
690 1 0 |a CARBOHYDRATES 
690 1 0 |a GALACTOFURANOSIDES 
690 1 0 |a GALACTOFURANOSYL ACCEPTORS 
690 1 0 |a GLYCOSYLATION 
690 1 0 |a ORGANIC SYNTHESIS 
690 1 0 |a CHEMISTRY TECHNIQUES, SYNTHETIC 
690 1 0 |a DRUG DESIGN 
690 1 0 |a GALACTOSE 
690 1 0 |a GLYCOCONJUGATES 
690 1 0 |a GLYCOSYLATION 
690 1 0 |a POLYSACCHARIDES 
700 1 |a Baldoni, L. 
773 0 |d 2014  |g v. 15  |h pp. 188-204  |k n. 2  |x 14397633  |t Chembiochem 
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856 4 0 |u https://hdl.handle.net/20.500.12110/paper_14397633_v15_n2_p188_Marino  |y Handle 
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