Convenient syntheses of 5-O- and 3,5-di-O-(β-d-galactofuranosyl)-d-galactofuranose

Benzoylation of d-galactono-1,4-lactone with 2.2 mol of benzoyl chloride, at -23°, gave the 2,6-dibenzoate (2, 62%). Tin(IV) chloride-catalyzed glycosylation of 2 with 1,2,3,5,6-penta-O-benzoyl-α,β-d-galactofuranose (1) afforded 2,6-di-O-benzoyl-5-O-(2,3,5,6-tetra-O-benzoyl-β-d-galactofuranosyl)-d-g...

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Detalles Bibliográficos
Autores principales:	de Lederkremer, R.M., Marino, C., Varela, O.
Formato:	JOUR
Materias:	3,5 di O (beta galactofuranosyl) galactofuranose 3,5-di-O-(beta-galactofuranosyl)-galactofuranose 5 O beta galactofuranosyl galactofuranose 5-O-beta-galactofuranosyl-galactofuranose disaccharide trisaccharide article carbohydrate analysis chemistry molecular genetics synthesis Carbohydrate Sequence Chemistry Disaccharides Molecular Sequence Data Support, Non-U.S. Gov't Trisaccharides
Acceso en línea:	http://hdl.handle.net/20.500.12110/paper_00086215_v200_nC_p227_deLederkremer
Aporte de:	Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) de Universidad de Buenos Aires

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