Author:
Džoganová Martina,Černý Miloslav,Buděšínský Miloš,Dračínský Martin,Trnka Tomáš
Abstract
Epoxide or pseudo-epoxide migration of 1,6:2,3-dianhydro- and 1,6:3,4-dianhydro-β-D-hexopyranoses was effected by treatment with aqueous sodium hydroxide or sodium iodide in acetone to give equilibrium mixtures. Various iodo derivatives of 1,6-anhydro-β-D-hexopyranoses were prepared as potential intermediates for pseudo-epoxide migration. NMR was used for following the reaction mechanism of epoxide and pseudo-epoxide migrations and analysis of reaction mixtures. Experimental data were compared with DFT calculations. Chair-boat equilibration of 1,6-anhydro-3-deoxy-3-halo-β-D-glucopyranoses was discussed.
Publisher
Institute of Organic Chemistry & Biochemistry
Cited by
5 articles.
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