The Reaction of Ammonia with Acylated Disaccharides. IV. The Structure of the 1,1-Bis(acetamido)-1-deoxyaldobiitols

By means of methylation and hydrolysis techniques it was demonstrated that the 1,1-bis(acetamido)-1-deoxycellobiitol, the 1,1-bis(acetamido)-1-deoxylactitol, and the 1,1-bis(acetamido)-1-deoxymaltitol obtained by the reaction of ammonia upon the corresponding acetylated aldobioses have an acyclic st...

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Autores principales: Deferrari, J.O., Cadenas, R.A.
Formato: JOUR
Acceso en línea:http://hdl.handle.net/20.500.12110/paper_00223263_v30_n6_p2007_Deferrari
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Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) de Universidad de Buenos Aires
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spelling todo:paper_00223263_v30_n6_p2007_Deferrari2023-10-03T14:31:13Z The Reaction of Ammonia with Acylated Disaccharides. IV. The Structure of the 1,1-Bis(acetamido)-1-deoxyaldobiitols Deferrari, J.O. Cadenas, R.A. By means of methylation and hydrolysis techniques it was demonstrated that the 1,1-bis(acetamido)-1-deoxycellobiitol, the 1,1-bis(acetamido)-1-deoxylactitol, and the 1,1-bis(acetamido)-1-deoxymaltitol obtained by the reaction of ammonia upon the corresponding acetylated aldobioses have an acyclic structure in the nitrogenated moiety. The separation of a mixture of 2,3,5,6-tetra-O-methyl-D-glucose and 2,3,4,6-tetra-O-methyl-D-glucose by gas-liquid and by anion-exchange resin chromatographies is described. © 1965, American Chemical Society. All rights reserved. Fil:Deferrari, J.O. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Cadenas, R.A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_00223263_v30_n6_p2007_Deferrari
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
description By means of methylation and hydrolysis techniques it was demonstrated that the 1,1-bis(acetamido)-1-deoxycellobiitol, the 1,1-bis(acetamido)-1-deoxylactitol, and the 1,1-bis(acetamido)-1-deoxymaltitol obtained by the reaction of ammonia upon the corresponding acetylated aldobioses have an acyclic structure in the nitrogenated moiety. The separation of a mixture of 2,3,5,6-tetra-O-methyl-D-glucose and 2,3,4,6-tetra-O-methyl-D-glucose by gas-liquid and by anion-exchange resin chromatographies is described. © 1965, American Chemical Society. All rights reserved.
format JOUR
author Deferrari, J.O.
Cadenas, R.A.
spellingShingle Deferrari, J.O.
Cadenas, R.A.
The Reaction of Ammonia with Acylated Disaccharides. IV. The Structure of the 1,1-Bis(acetamido)-1-deoxyaldobiitols
author_facet Deferrari, J.O.
Cadenas, R.A.
author_sort Deferrari, J.O.
title The Reaction of Ammonia with Acylated Disaccharides. IV. The Structure of the 1,1-Bis(acetamido)-1-deoxyaldobiitols
title_short The Reaction of Ammonia with Acylated Disaccharides. IV. The Structure of the 1,1-Bis(acetamido)-1-deoxyaldobiitols
title_full The Reaction of Ammonia with Acylated Disaccharides. IV. The Structure of the 1,1-Bis(acetamido)-1-deoxyaldobiitols
title_fullStr The Reaction of Ammonia with Acylated Disaccharides. IV. The Structure of the 1,1-Bis(acetamido)-1-deoxyaldobiitols
title_full_unstemmed The Reaction of Ammonia with Acylated Disaccharides. IV. The Structure of the 1,1-Bis(acetamido)-1-deoxyaldobiitols
title_sort reaction of ammonia with acylated disaccharides. iv. the structure of the 1,1-bis(acetamido)-1-deoxyaldobiitols
url http://hdl.handle.net/20.500.12110/paper_00223263_v30_n6_p2007_Deferrari
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AT deferrarijo reactionofammoniawithacylateddisaccharidesivthestructureofthe11bisacetamido1deoxyaldobiitols
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