Cyclization of<i>N</i>(Tetra-<i>O</i>-acetyl-<scp>d</scp>-gluco- and<scp>d</scp>-Mannopyranosyl)-Pyridinium Salts in a Methanolic Solution of Sodium Methylate

Abstract

Abstract N-(2,3,4,6-Tetra-O-acetyl-α-d-gluco-, β-d-gluco- and β-d-mannopyranosyl)-pyridinium salts were obtained and their structures were determined by 2D 1H NMR spectroscopy. The compounds obtained were treated with a methanolic solution of sodium methylate. The β-anomer of the d-gluco derivative cyclizes via Brigl's anhydride but the α anomer is competitively transformed according to the SN2 and SN1 mechanisms. The β-d-manno derivative does not cyclize under the conditions used. Comparison of the qualitative and quantitative results of the reaction studied enabled estimation of the influence of configuration at C-1 and C-2 on the course of cyclization. All product mixtures were separated by capillary gas chromatography (CGC) as exhaustively O-acetylated derivatives and their components were identified by coinjection with authentic materials.