Sugars: Intramolecular Dehydration of Hexoses - Université de Reims Champagne-Ardenne
Chapitre D'ouvrage Année : 2021

Sugars: Intramolecular Dehydration of Hexoses

Résumé

If the definition of saccharides (or sugars) is rather unclear, specialists usually agree on saying that chemists can describe saccharides as structures derived from chiral entities bearing hydroxyl or diversely substituted hydroxyl, incorporating in this family molecules with nitrogen, sulphur or even alkyl, inspired by a Fischer-type skeleton. Because this is only limited by our imagination, chemists may generally say that saccharide derivatives should look like saccharides (joke). However, we agree on an unanimous definition for “hexoses”: simple sugars containing six carbon atoms and the equivalent of one molecule of water per carbon atom (C,H2O)6 or C6H12O6 in their general formula. All D-hexoses are naturally occurring, with the exception of D-altrose, the major ones being D-glucose, D-galactose, D-mannose and D-fructose

Domaines

Chimie organique
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Dates et versions

hal-03552244 , version 1 (02-02-2022)

Identifiants

Citer

Marie-Charlotte Belhomme, Stéphanie Castex, Arnaud Haudrechy. Sugars: Intramolecular Dehydration of Hexoses. Christophe Lavelle, Herve This, Alan L. Kelly, Roisin Burke. Handbook of Molecular Gastronomy, 1, CRC Press, pp.563-568, 2021, 9780429168703. ⟨10.1201/9780429168703-86⟩. ⟨hal-03552244⟩
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