## Abstract __S__‐Methylation of 6‐__S__‐benzyl‐6‐deoxy‐1,2‐__O__‐isopropylidene‐3‐__O__‐methyl‐α‐D‐__xylo__‐6‐thiohexofuranos‐5‐ulose (**1**) gave the expected sulfonium salt **2** which on alcaline treatment yielded the stable sulfur ylide **3**. This compound constitutes an useful synthetic inte
Dérivés diglycosyliques. Communication préliminaire
✍ Scribed by Jean M. J. Tronchet; Ford Habashi; Olivier R. Martin; Alain P. Bonenfant; Bruno Baehler; Jean-Bernard Zumwald
- Publisher
- John Wiley and Sons
- Year
- 1979
- Tongue
- German
- Weight
- 231 KB
- Volume
- 62
- Category
- Article
- ISSN
- 0018-019X
No coin nor oath required. For personal study only.
✦ Synopsis
Diglycosyl Derivatives. Preliminary communication
Novel types of diglycosyl compounds, some of them bearing a resemblance to natural di‐ or tri‐saccharides are described: a diglycosyldiyne (1), a diglycosylthiophene (2), a diglycosylaziridine (3), a diglycosyldioxolane (4), as well as six C,N‐diglycosylnitrones, 9b–9f and 14. These C,N‐diglycosylnitrones, on treatment with an acetylenic Grignard reagent, led to the expected acetylenic diglycosyl‐hydroxylamine 11, whereas diglycosylisoxazolines (f. ex. 10) were obtained when these nitrones underwent 1,3‐dipolar cycloaddition to acetylenic compounds.
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