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, Jorge O., Thiel, Inge María E., Cadenas, Raúl Alberto
Publicado: 1965
Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00223263_v30_n9_p3053_Deferrari
http://hdl.handle.net/20.500.12110/paper_00223263_v30_n9_p3053_Deferrari
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spelling paper:paper_00223263_v30_n9_p3053_Deferrari2023-06-08T14:49:24Z The reaction of ammonia with acylated disaccharides. VI. Octa-O-benzoylcellobiose and benzoyl derivatives of cellobiose Deferrari, Jorge O. Thiel, Inge María E. Cadenas, Raúl Alberto 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. 1965 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00223263_v30_n9_p3053_Deferrari 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)
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.
author Deferrari, Jorge O.
Thiel, Inge María E.
Cadenas, Raúl Alberto
spellingShingle Deferrari, Jorge O.
Thiel, Inge María E.
Cadenas, Raúl Alberto
The reaction of ammonia with acylated disaccharides. VI. Octa-O-benzoylcellobiose and benzoyl derivatives of cellobiose
author_facet Deferrari, Jorge O.
Thiel, Inge María E.
Cadenas, Raúl Alberto
author_sort Deferrari, Jorge 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
publishDate 1965
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00223263_v30_n9_p3053_Deferrari
http://hdl.handle.net/20.500.12110/paper_00223263_v30_n9_p3053_Deferrari
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