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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Publicado: 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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spelling 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