Partial oxyamination of 4,6-di-0-acetyl-2,3-dideoxy-cu-D-erythro-hex-2enopyranosyl 4,6-di-O-acetyl-2,3-dideoxy-a-D-erythro-hex-Zenopyranoside with chloramine-T and osmium tetraoxide gave 4,6-di-0-acetyl-2-deoxy-2-(p-toluenesulfonamide)-a-D-mannopyranosyl 4,6-di-0-acetyl-2,3-dideoxy-ry-D-erythro-hex-
✦ LIBER ✦
Synthesis of 2-deoxy, 3-deoxy, and 2,3-dideoxy analogs of α,α-trehalose by reductive desulfonyloxylation of p-toluenesulfonates with lithium triethylborohydride
✍ Scribed by Hans H. Baer; Miroslawa Mekarska; Francine Boucher
- Publisher
- Elsevier Science
- Year
- 1985
- Tongue
- English
- Weight
- 829 KB
- Volume
- 136
- Category
- Article
- ISSN
- 0008-6215
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