A convenient and general approach to the synthesis of properly protected d-nucleoside-3′-hydrogenphosphonates via phosphite intermediates
✍ Scribed by J.E Marugg; M Tromp; E Kuyl-Yeheskiely; G.A van der Marel; J.H van Boom
- Publisher
- Elsevier Science
- Year
- 1986
- Tongue
- French
- Weight
- 246 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
Evidence will be presented to show that the monofunctional phosphitylating reagents bis(N,N-di-ethylamino)chlorophosphine and salicylchlorophosphine are very effective for the preparation of 5'-O,N-protected d-nucleoside-3'-hydrogenphosphonates.
📜 SIMILAR VOLUMES
2-Deoxy-D-glucitol and 2-deoxy-D-allitol, both prepared as crystalline polyols from D-erythronolactone, are oxidized by Gluconobacter thailandicus NBRC 3254 to 5-deoxy-D-threo-hexulose [5-deoxy-D-fructose = 5-deoxy-L-sorbose] and 5-deoxy-D-erythro-hexulose [5-deoxy-L-psicose = 5-deoxy-D-tagatose], r