Enantiomerically pure 7-OxdbiCyClO[2.2.I]hept-5-en-2-yl derivatives ('naked sugars') as synthetic intermediates, Part V. Part 111: [l]. Part IV: [2]. Part of the planned Ph.D. thesis of F. G., University of Lausanne.
Synthesis of amino-1,4-anhydro-d-pentitols and amino-1,5-anhydro-d-hexitols with the arabino configuration from (R)-glycidol
✍ Scribed by Sı́lvia Aragonès; Fernando Bravo; Yolanda Dı́az; Ma̱ Isabel Matheu; Sergio Castillón
- Book ID
- 104359864
- Publisher
- Elsevier Science
- Year
- 2003
- Tongue
- English
- Weight
- 227 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0957-4166
No coin nor oath required. For personal study only.
✦ Synopsis
2-Amino-1,4-anhydro-pentitol and 3-amino-1,5-anhydro-4-deoxy-hexitol with the arabino configuration were synthesised from (R)-glycidol using a metathesis reaction as the key step. The dihydrofuran or dihydropyran products obtained after the metathesis reaction were subjected to epoxidation, epoxide opening with azide anion and finally azide reduction.
📜 SIMILAR VOLUMES
Homo-C-nucleoside Analogues. Part 2. Synthesis and Anomeric Configuration of 4-(2,5-Anhydro-D-gluco-pentitol-1-yl)-2-phenyl-2H-1,2,3-triazole. -The configuration of the title compound (III) is determined by acetylation and by spectroscopical means. -(SALLAM, M. A.