Preparation of O-, S- and N-Benzyl Derivatives of 1,6-Anhydro-beta-D-hexopyranoses via Aziridine Ring Opening

Abstrakt

The aziridine ring opening of N-tosylepimino carbohydrates having D-allo, D-manno, D-galacto and D-talo configurations with benzyl alcohol, benzylamine and phenylmethanethiol have been studied.

Klíčová slova

• carbohydrates
• ring opening reactions
• stereospecific synthesis
• NMR spectroscopy
• aziridines