Efficient Synthesis of Sugar 3,2‐Enolones from 2‐Hydroxyglycals and Their Conversion into 4‐Pyrones

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Efficient Synthesis of Sugar 3,2‐Enolones from 2‐Hydroxyglycals and Their Conversion into 4‐Pyrones

Abstract: Fig. I. Structure of the cation [O(Hgl)zHgOH]-; bond lengths [pm] and bond angles ["I.

Cited by 3 publications

References 15 publications

Preparation of some acylated 4-deoxyhex-3-enopyranosiduloses and γ-pyrone formation therefrom

Preparation of some acylated 4-deoxyhex-3-enopyranosiduloses and γ-pyrone formation therefrom

Syntheses of derivatives of p-aminophenyl 3-O-(3,6-dideoxy-α-d-arabino- and α-d-ribo-hexopyranosyl)-α-d-mannopyranosides by use of hydroxyglycal intermediates

Preparation and some reactions of benzoylated 4-deoxy-d-glycero-hex-3-enos-2-uloses

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