β-Elimination in aldonolactones: a convenient synthesis of 2-deoxy-D-erythro-pentose
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference11 articles.
1. β-Elimination in aldonolactones: a convenient synthesis of 2,4,6-tri-O-benzoyl-3-deoxy-D-arabino-hexono-1,5-lactone
2. 2-Deoxy-D-ribose. VI.1 The Preparation of Derivatives of 3-Deoxy-D-ribo-hexonic Acid and 3-Deoxy-D-arabino-hexonic Acid Therefrom. Some Observations on the Kiliani Synthesis
3. ENZYMATIC PREPARATION OF α-KETO ACIDS
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1. Descending syntheses of monosaccharides;Monosaccharide Sugars;1998
2. Synthetic Reactions of Aldonolactones;Advances in Carbohydrate Chemistry and Biochemistry;1994
3. Fumarase-catalyzed synthesis of L-threo-chloromalic acid and its conversion to 2-deoxy-D-ribose and D-erythro-sphingosine;The Journal of Organic Chemistry;1987-06
4. Crystalline furanose derivatives of 3-deoxy-d-arabino-hexose: Conformational studies by n.m.r. spectroscopy;Carbohydrate Research;1985-06
5. A New Synthesis of 3-Deoxy-D-arabino-hexose and its Tautomeric Equilibrium;Journal of Carbohydrate Chemistry;1984-01
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