Comprehensive Reinvestigation of The Reaction of D-Aldoses With Meldrum'S Acid Yielding Mainly Chain Extended 3,6-Anhydro-2-Deoxy-Aldono-1,4-Lactones
Author:
Affiliation:
1. a University of Oldenburg, Department of Chemistry , P.O.Box 2503, D-26111 Oldenburg, Germany
2. b Prochem Research and Development Ltd. , P.O. Box 17, H-1525 Budapest, Hungary
Publisher
Informa UK Limited
Subject
Organic Chemistry,Biochemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/07328300008544132
Reference6 articles.
1. Györgydeák , Z. and Pelyvás , I. F. 1997. Monosaccharide Sugars: Chemical Synthesis by Chain Elongation, Degradation, and Epimerisation, 3–373. San Diego: Academic Press.
2. A facile synthesis of C-glycosylbarbiturates
3. Reaction of sugars with Meldrum's acid: A route to 3,6-anhydro-2-deoxyaldono-1,4-lactones
4. LIV.—A β-lactonic acid from acetone and malonic acid
5. Transformation of aldoses into glycosylamine 1,2-(cyclic carbamates) (glyco-oxazolidin-2-ones) by reaction with potassium cyanate
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