Separation and quantitation of enantiomeric 3,6-anhydrogalactoses by conversion to the corresponding diastereomeric acetylated sec-butyl 3,6-anhydrogalactonates
A method to determine the proportion of both enantiomers of 3,6-anhydrogalactose in a sample has been developed using methyl 3,6-anhydro-α-d-galactoside as a model compound. It involves an oxidative hydrolysis to obtain the corresponding aldonic acids, which are further converted to the acetylated d...
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1998
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Acceso en línea: | https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00086215_v311_n4_p235_Errea http://hdl.handle.net/20.500.12110/paper_00086215_v311_n4_p235_Errea |
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paper:paper_00086215_v311_n4_p235_Errea2023-06-08T14:32:37Z Separation and quantitation of enantiomeric 3,6-anhydrogalactoses by conversion to the corresponding diastereomeric acetylated sec-butyl 3,6-anhydrogalactonates 3,6-Anhydrogalactonic acids 3,6-Anhydrogalactonic acids, sec-butyl esters 3,6-Anhydrogalactose 3,6-Anhydrogalactose, enantiomers Seaweed polysaccharides galactose polysaccharide article carbohydrate synthesis diastereoisomer enantiomer hydrolysis oxidation priority journal seaweed A method to determine the proportion of both enantiomers of 3,6-anhydrogalactose in a sample has been developed using methyl 3,6-anhydro-α-d-galactoside as a model compound. It involves an oxidative hydrolysis to obtain the corresponding aldonic acids, which are further converted to the acetylated diastereomeric sec-butyl esters. These are separated and quantified by GLC using a standard column for carbohydrate analysis; the procedure has been extended to seaweed polysaccharides. Copyright (C) 1998 Elsevier Science Ltd. 1998 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00086215_v311_n4_p235_Errea http://hdl.handle.net/20.500.12110/paper_00086215_v311_n4_p235_Errea |
institution |
Universidad de Buenos Aires |
institution_str |
I-28 |
repository_str |
R-134 |
collection |
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) |
topic |
3,6-Anhydrogalactonic acids 3,6-Anhydrogalactonic acids, sec-butyl esters 3,6-Anhydrogalactose 3,6-Anhydrogalactose, enantiomers Seaweed polysaccharides galactose polysaccharide article carbohydrate synthesis diastereoisomer enantiomer hydrolysis oxidation priority journal seaweed |
spellingShingle |
3,6-Anhydrogalactonic acids 3,6-Anhydrogalactonic acids, sec-butyl esters 3,6-Anhydrogalactose 3,6-Anhydrogalactose, enantiomers Seaweed polysaccharides galactose polysaccharide article carbohydrate synthesis diastereoisomer enantiomer hydrolysis oxidation priority journal seaweed Separation and quantitation of enantiomeric 3,6-anhydrogalactoses by conversion to the corresponding diastereomeric acetylated sec-butyl 3,6-anhydrogalactonates |
topic_facet |
3,6-Anhydrogalactonic acids 3,6-Anhydrogalactonic acids, sec-butyl esters 3,6-Anhydrogalactose 3,6-Anhydrogalactose, enantiomers Seaweed polysaccharides galactose polysaccharide article carbohydrate synthesis diastereoisomer enantiomer hydrolysis oxidation priority journal seaweed |
description |
A method to determine the proportion of both enantiomers of 3,6-anhydrogalactose in a sample has been developed using methyl 3,6-anhydro-α-d-galactoside as a model compound. It involves an oxidative hydrolysis to obtain the corresponding aldonic acids, which are further converted to the acetylated diastereomeric sec-butyl esters. These are separated and quantified by GLC using a standard column for carbohydrate analysis; the procedure has been extended to seaweed polysaccharides. Copyright (C) 1998 Elsevier Science Ltd. |
title |
Separation and quantitation of enantiomeric 3,6-anhydrogalactoses by conversion to the corresponding diastereomeric acetylated sec-butyl 3,6-anhydrogalactonates |
title_short |
Separation and quantitation of enantiomeric 3,6-anhydrogalactoses by conversion to the corresponding diastereomeric acetylated sec-butyl 3,6-anhydrogalactonates |
title_full |
Separation and quantitation of enantiomeric 3,6-anhydrogalactoses by conversion to the corresponding diastereomeric acetylated sec-butyl 3,6-anhydrogalactonates |
title_fullStr |
Separation and quantitation of enantiomeric 3,6-anhydrogalactoses by conversion to the corresponding diastereomeric acetylated sec-butyl 3,6-anhydrogalactonates |
title_full_unstemmed |
Separation and quantitation of enantiomeric 3,6-anhydrogalactoses by conversion to the corresponding diastereomeric acetylated sec-butyl 3,6-anhydrogalactonates |
title_sort |
separation and quantitation of enantiomeric 3,6-anhydrogalactoses by conversion to the corresponding diastereomeric acetylated sec-butyl 3,6-anhydrogalactonates |
publishDate |
1998 |
url |
https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00086215_v311_n4_p235_Errea http://hdl.handle.net/20.500.12110/paper_00086215_v311_n4_p235_Errea |
_version_ |
1768543590465667072 |