New syntheses of d-tagatose and of 1,5-anhydro-d-tagatose from d-galactose derivatives
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference27 articles.
1. A facile conversion of 3,4-O-isopropylidene-β-d-galactopyranosides into 4-deoxy-α-l-threo-hex-4-enopyranoside and l-arabino-hexos-5-ulose derivatives
2. A simple stereospecific route to 5-C-alkoxy-D-galactopyransides and to L-arabino-hexos-5-uloses
3. A new synthesis of L-ascorbic acid from D-galactose
4. Synthesis of 2,6-anhydro-3-deoxy-l-threo-hex-2-enitol (“l-sorbal”) and of l-tagatose from d-galactose
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3. Furo[2,3-c]pyrans from a Vinyl Sulfone Modified Methyl 2,6-O-Anhydro-α-D-hexopyranoside: An Experimental and Theoretical Investigation;European Journal of Organic Chemistry;2013-10-25
4. Creation of Metal-Independent Hyperthermophilic l-Arabinose Isomerase by Homologous Recombination;Journal of Agricultural and Food Chemistry;2011-12-06
5. ChemInform Abstract: Rare and Complex Saccharides from D-Galactose and Other Milk-Derived Carbohydrates. Part 5. New Syntheses of D-Tagatose and of 1,5-Anhydro- D-tagatose from D-Galactose Derivatives.;ChemInform;2010-08-12
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