The reaction of ammonia with acylated disaccharides. VI. Octa-O-benzoylcellobiose and benzoyl derivatives of cellobiose

β-Octa-O-benzoylcellobiose (I) was prepared and, from its reaction with methanolic ammonia, cellobiose (II), 4-O-β-D-glucopyranosyl-1,1-bis(benzamido)-1-deoxy-D-glucitol (IIIa), N-benzoylcellobiosylamine (IVa), and 6-O-benzoylcellobiose (V) were obtained. The structure of compounds IIIa and V were e...

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Autores principales: Deferrari, J.O., Thiel, I.M.E., Cadenas, R.A.
Formato: JOUR
Lenguaje:English
Acceso en línea:http://hdl.handle.net/20.500.12110/paper_00223263_v30_n9_p3053_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_n9_p3053_Deferrari2023-10-03T14:31:13Z The reaction of ammonia with acylated disaccharides. VI. Octa-O-benzoylcellobiose and benzoyl derivatives of cellobiose Deferrari, J.O. Thiel, I.M.E. Cadenas, R.A. β-Octa-O-benzoylcellobiose (I) was prepared and, from its reaction with methanolic ammonia, cellobiose (II), 4-O-β-D-glucopyranosyl-1,1-bis(benzamido)-1-deoxy-D-glucitol (IIIa), N-benzoylcellobiosylamine (IVa), and 6-O-benzoylcellobiose (V) were obtained. The structure of compounds IIIa and V were established. Fil:Deferrari, J.O. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Thiel, I.M.E. 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 English info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_00223263_v30_n9_p3053_Deferrari
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
language English
orig_language_str_mv English
description β-Octa-O-benzoylcellobiose (I) was prepared and, from its reaction with methanolic ammonia, cellobiose (II), 4-O-β-D-glucopyranosyl-1,1-bis(benzamido)-1-deoxy-D-glucitol (IIIa), N-benzoylcellobiosylamine (IVa), and 6-O-benzoylcellobiose (V) were obtained. The structure of compounds IIIa and V were established.
format JOUR
author Deferrari, J.O.
Thiel, I.M.E.
Cadenas, R.A.
spellingShingle Deferrari, J.O.
Thiel, I.M.E.
Cadenas, R.A.
The reaction of ammonia with acylated disaccharides. VI. Octa-O-benzoylcellobiose and benzoyl derivatives of cellobiose
author_facet Deferrari, J.O.
Thiel, I.M.E.
Cadenas, R.A.
author_sort Deferrari, J.O.
title The reaction of ammonia with acylated disaccharides. VI. Octa-O-benzoylcellobiose and benzoyl derivatives of cellobiose
title_short The reaction of ammonia with acylated disaccharides. VI. Octa-O-benzoylcellobiose and benzoyl derivatives of cellobiose
title_full The reaction of ammonia with acylated disaccharides. VI. Octa-O-benzoylcellobiose and benzoyl derivatives of cellobiose
title_fullStr The reaction of ammonia with acylated disaccharides. VI. Octa-O-benzoylcellobiose and benzoyl derivatives of cellobiose
title_full_unstemmed The reaction of ammonia with acylated disaccharides. VI. Octa-O-benzoylcellobiose and benzoyl derivatives of cellobiose
title_sort reaction of ammonia with acylated disaccharides. vi. octa-o-benzoylcellobiose and benzoyl derivatives of cellobiose
url http://hdl.handle.net/20.500.12110/paper_00223263_v30_n9_p3053_Deferrari
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AT cadenasra thereactionofammoniawithacylateddisaccharidesvioctaobenzoylcellobioseandbenzoylderivativesofcellobiose
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