## Abstract __Cis__ and __trans__‐methyl‐4‐deoxy‐2, 3‐O‐isopropylidene‐6‐O‐methyl‐4‐methylthio‐methylene‐α‐D‐__lyxo__‐hexopyra‐nosides are prepared by a __Wittig__ reaction. Methods are described for the determination of the configuration of the geometrical isomers whose __Raney__‐Nickel reduction
Utilisation d'ylides du phosphore non stabilisés en chimie des sucres. II. Action du méthylthiométhylène-triphénylphosphorane sur les aldéhydo-surces
✍ Scribed by J. M. J. Tronchet; Mme S. Jaccard-Thorndahl; Br. Baehler
- Publisher
- John Wiley and Sons
- Year
- 1969
- Tongue
- German
- Weight
- 289 KB
- Volume
- 52
- Category
- Article
- ISSN
- 0018-019X
No coin nor oath required. For personal study only.
✦ Synopsis
10 Boulebard d'Yboy, 1205 G e n h c (24 TIT 69)
Suvn~nnary. The action of methplthioiiicthylene-triphenylphosphorane on 2,3:4,5-di-(I-isopropylidene-aldehyde-1.-arabinose Icd with good yields to t h c corresponding unsaturatcd sugar which underwent electrophilic addition with a high regiospecificity. This provides a useful ncw route for a one-carbon chain extension in the carbohydrate series.
📜 SIMILAR VOLUMES
## Abstract The previously described one‐carbon chain extension of __aldehydo__‐sugars with methylthiomethylene‐triphenylphosphorane has been successfully applied to an anhydro‐__aldehydo__‐sugar and two __w__‐__aldehydo__‐sugars. Some spectroscopic properties of the so obtained methylthiovinylic s