Reaction of ammonia with some acetylated and benzoylated monosaccharides. Part XII.N-acyl-D-glucosylamines and 1, 1-bis(acylamido)-1-deoxy-D-glucitols isolated from the ammonolysis of different penta-O-acyl-D-glucoses
NewN-acyl-D-glucosylamines (2,3) and 1,1-bis(acylamido)-1-deoxy-D-glucitols (1) have been isolated by applying chromatographic and ionophoretic techniques to the separation of the products from the ammonolysis of penta-O-acetyl-, penta-O-propionyl-, and penta-O-benzoyl-D-glucopyranose. It has been f...
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1968
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Acceso en línea: | https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00086215_v7_n4_p395_Cerezo http://hdl.handle.net/20.500.12110/paper_00086215_v7_n4_p395_Cerezo |
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paper:paper_00086215_v7_n4_p395_Cerezo2023-06-08T14:33:10Z Reaction of ammonia with some acetylated and benzoylated monosaccharides. Part XII.N-acyl-D-glucosylamines and 1, 1-bis(acylamido)-1-deoxy-D-glucitols isolated from the ammonolysis of different penta-O-acyl-D-glucoses Cerezo, Alberto Saúl Sproviero, Jorge Félix Deulofeu, Venancio Delpy, Susana M. NewN-acyl-D-glucosylamines (2,3) and 1,1-bis(acylamido)-1-deoxy-D-glucitols (1) have been isolated by applying chromatographic and ionophoretic techniques to the separation of the products from the ammonolysis of penta-O-acetyl-, penta-O-propionyl-, and penta-O-benzoyl-D-glucopyranose. It has been found that, in all cases, acyclic (1) and cyclic (2, 3) products are formed simultaneously. The molar ratio of the cyclic products formed (2+3) to the acyclic ones (1) is higher if the acyl group is aliphatic. The yield ofN-benzoyl-β-D-mannopyranosylamine obtained in the ammonolysis of penta-O-benzoyl-D-mannopyranose is higher than that ofN-benzoyl-β-D-glucopyranosylamine from penta-O-benzoyl-D-glucopyranose, showing the influence of inversion of configuration at C-2. This influence is less pronounced for other acylated monosaccharides that belong to themanno series. © 1968 Elsevier Publishing Company, Amsterdam. Fil:Cerezo, A.S. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Sproviero, J.F. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Deulofeu, V. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Delpy, S. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 1968 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00086215_v7_n4_p395_Cerezo http://hdl.handle.net/20.500.12110/paper_00086215_v7_n4_p395_Cerezo |
institution |
Universidad de Buenos Aires |
institution_str |
I-28 |
repository_str |
R-134 |
collection |
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) |
description |
NewN-acyl-D-glucosylamines (2,3) and 1,1-bis(acylamido)-1-deoxy-D-glucitols (1) have been isolated by applying chromatographic and ionophoretic techniques to the separation of the products from the ammonolysis of penta-O-acetyl-, penta-O-propionyl-, and penta-O-benzoyl-D-glucopyranose. It has been found that, in all cases, acyclic (1) and cyclic (2, 3) products are formed simultaneously. The molar ratio of the cyclic products formed (2+3) to the acyclic ones (1) is higher if the acyl group is aliphatic. The yield ofN-benzoyl-β-D-mannopyranosylamine obtained in the ammonolysis of penta-O-benzoyl-D-mannopyranose is higher than that ofN-benzoyl-β-D-glucopyranosylamine from penta-O-benzoyl-D-glucopyranose, showing the influence of inversion of configuration at C-2. This influence is less pronounced for other acylated monosaccharides that belong to themanno series. © 1968 Elsevier Publishing Company, Amsterdam. |
author |
Cerezo, Alberto Saúl Sproviero, Jorge Félix Deulofeu, Venancio Delpy, Susana M. |
spellingShingle |
Cerezo, Alberto Saúl Sproviero, Jorge Félix Deulofeu, Venancio Delpy, Susana M. Reaction of ammonia with some acetylated and benzoylated monosaccharides. Part XII.N-acyl-D-glucosylamines and 1, 1-bis(acylamido)-1-deoxy-D-glucitols isolated from the ammonolysis of different penta-O-acyl-D-glucoses |
author_facet |
Cerezo, Alberto Saúl Sproviero, Jorge Félix Deulofeu, Venancio Delpy, Susana M. |
author_sort |
Cerezo, Alberto Saúl |
title |
Reaction of ammonia with some acetylated and benzoylated monosaccharides. Part XII.N-acyl-D-glucosylamines and 1, 1-bis(acylamido)-1-deoxy-D-glucitols isolated from the ammonolysis of different penta-O-acyl-D-glucoses |
title_short |
Reaction of ammonia with some acetylated and benzoylated monosaccharides. Part XII.N-acyl-D-glucosylamines and 1, 1-bis(acylamido)-1-deoxy-D-glucitols isolated from the ammonolysis of different penta-O-acyl-D-glucoses |
title_full |
Reaction of ammonia with some acetylated and benzoylated monosaccharides. Part XII.N-acyl-D-glucosylamines and 1, 1-bis(acylamido)-1-deoxy-D-glucitols isolated from the ammonolysis of different penta-O-acyl-D-glucoses |
title_fullStr |
Reaction of ammonia with some acetylated and benzoylated monosaccharides. Part XII.N-acyl-D-glucosylamines and 1, 1-bis(acylamido)-1-deoxy-D-glucitols isolated from the ammonolysis of different penta-O-acyl-D-glucoses |
title_full_unstemmed |
Reaction of ammonia with some acetylated and benzoylated monosaccharides. Part XII.N-acyl-D-glucosylamines and 1, 1-bis(acylamido)-1-deoxy-D-glucitols isolated from the ammonolysis of different penta-O-acyl-D-glucoses |
title_sort |
reaction of ammonia with some acetylated and benzoylated monosaccharides. part xii.n-acyl-d-glucosylamines and 1, 1-bis(acylamido)-1-deoxy-d-glucitols isolated from the ammonolysis of different penta-o-acyl-d-glucoses |
publishDate |
1968 |
url |
https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00086215_v7_n4_p395_Cerezo http://hdl.handle.net/20.500.12110/paper_00086215_v7_n4_p395_Cerezo |
work_keys_str_mv |
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1768545077231091712 |