Preparation of partially O-methylated alditol acetate standards of allose, altrose, gulose and talose for GC–MS analysis of structures containing rare sugars

Mixtures of partially O-methylated alditol acetate standards of allose, altrose, gulose and talose were synthesised. Methyl glycosides of each sugar were prepared and partially methylated using the NaOH/DMSO methylation procedure, adding 0.75 hydroxyl group equivalents of CH<sub>3</sub>I. Following conversion to partially methylated alditol acetates, via successive hydrolysis, reduction, and acetylation, the derivatives were separated by gas chromatography on low and high polarity columns and analysed by electron impact mass spectrometry. Detailed data on retention times relative to myo-inositol hexaacetate on the two columns are provided.

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Publication Details

Journal
Carbohydrate Research
Published
2025-05-08
DOI
https://doi.org/10.1016/j.carres.2025.109513
Citations
2
Primary Topic
Diet, Metabolism, and Disease
Type
article
Field-Weighted Citation Impact
2.59

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article

Preparation of partially O-methylated alditol acetate standards of allose, altrose, gulose and talose for GC–MS analysis of structures containing rare sugars

Cara A. Luiten, Simon F.R. Hinkley, Tracey Bell, Ian M. Sims et al.
2 citations
Carbohydrate Research
Diet, Metabolism, and Disease
2.59
article

Preparation of partially O-methylated alditol acetate standards of allose, altrose, gulose and talose for GC–MS analysis of structures containing rare sugars

Cara A. Luiten, Simon F.R. Hinkley, Tracey Bell, Ian M. Sims, Carmen Muñoz
article en
2 citations

Abstract

Mixtures of partially O-methylated alditol acetate standards of allose, altrose, gulose and talose were synthesised. Methyl glycosides of each sugar were prepared and partially methylated using the NaOH/DMSO methylation procedure, adding 0.75 hydroxyl group equivalents of CH<sub>3</sub>I. Following conversion to partially methylated alditol acetates, via successive hydrolysis, reduction, and acetylation, the derivatives were separated by gas chromatography on low and high polarity columns and analysed by electron impact mass spectrometry. Detailed data on retention times relative to myo-inositol hexaacetate on the two columns are provided.

Carbohydrate ResearchVol. 553
Victoria University of Wellington (NZ)
Ministry of Business, Innovation and Employment
Zero hunger
Openalex Percentile: Top 10%
Diet, Metabolism, and Disease
2.59
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Preparation of partially O-methylated alditol acetate standards of allose, altrose, gulose and talose for GC–MS analysis of structures containing rare sugars — Cara A. Luiten, Simon F.R. Hinkley, et al. · Carbohydrate Research (2025) | TGRS Research Map | TGRS