β-Elimination in aldonolactones. the conversion of l-rhamnono-1-5-lactone into 3-benzoyloxy-6-methylpyran-2-one
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference13 articles.
1. The formation of an unsaturated lactone derivative on benzoylation of D-galactonolactone
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3. β-Elimination in aldonolactones: a convenient synthesis of 2,4,6-tri-O-benzoyl-3-deoxy-D-arabino-hexono-1,5-lactone
4. β-Elimination in aldonolactones. Synthesis of 3,6-dideoxy L-arabino-hexose (ascarylose)
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1. Pyrone Synthesis from Renewable Sources: Easy Preparation of 3-Acetoxy-2-oxo-2H-pyran-6-carboxylic Salts and their Derivatives as 3-Hydroxy-2H-pyran-2-one from C6 Aldaric Acids;European Journal of Organic Chemistry;2020-01-09
2. Chemical synthesis of GDP-l-galactose and analogues;Carbohydrate Research;1998-01
3. A Carbohydrate Approach to the Enantioselective Synthesis of 1,3-Polyols;The Journal of Organic Chemistry;1996-01-01
4. Synthetic Reactions of Aldonolactones;Advances in Carbohydrate Chemistry and Biochemistry;1994
5. One-pot conversion of O-acetylsugar lactones into 2,3-dideoxysugar derivatives via platinum-catalyzed hydrogenolysis;Tetrahedron Letters;1991-09
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