Abstract
ABSTRACT All diastereomeric aldo-D-pentoses and -D-hexoses were reacted with Meldrum's acid (2,2-dimethyl-1,3-dioxane-4,6-dione) under basic conditions. A protocol was applied and optimized which was originally reported by J. A. Galbis Perez et al. in 1990. In every case formal substitution of the anomeric hydroxyl against a carboxy-methylene group occurred thus elongating the carbon chain of the parent aldose by a C2 fragment. Products are mainly 3,6-anhydro-2-deoxy-aldono-1,4-lactones in which the lactone rings are annulated to a furanoid system. However, D-mannose and D-lyxose also gave pyranoid 3,7-anhydro-1,4-lactones. Intermediates are unsaturated open-chain 1,4-lactones (butenolides) which in some cases could be isolated as by-products. Epimerisation at C-2 of the parent aldose occurred at least partially in most reactions. The products and their acetylated derivatives were characterized by 1H and 13C NMR spectroscopy. A proposed mechanism of this reaction is supported by additional experimental evidence.
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