The title compound (21) was synthesized from cellobiose as a synthon of a heparin-related oligosaccharide. The per-0-benzyl and per-0-benzoyl derivatives of 1 ,6-anhydro-4-0-(6-deoxy-B-D-~~~lo-hex-5-enopyranosyl)-~-~-glucopyranose were treated with a nonsolvated borane to give a 1 :2 mixture of the
Preparation of 2,5-anhydro-3,4,6-tri-O-benzoyl-d-allononitrile from d-glucose
✍ Scribed by Mirjana Popsavin; Velimir Popsavin; Nada Vukojević; János Csanádi; Dušan Miljković
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- English
- Weight
- 484 KB
- Volume
- 260
- Category
- Article
- ISSN
- 0008-6215
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From 2,4,6-tri-da-methylpyryliurn perchlorate the title compounds II-V were obtained by reaction with aqueous or gaseous ammonia, aqueous sodium hydroxide, aqueous hydrogen peroxide and sodium cyclopentadienide, respectively. The preparation of II-IV in aqueous solution proves that the nucleophilic
## Abstract 1,4‐Anhydro‐2,3,6‐tri‐__O__‐benzyl‐α‐D‐glucopyranose **(1)** wird mit Triäthyloxonium‐tetra‐fluoroborat **(2)** zu einem linearen 2,3,6‐Tri‐__O__‐benzyl‐β(1 → 4)‐polysaccharid polymerisiert. Dies enthält einen geringen Teil α(1 → 4)‐Bindungen. Abspaltung der Benzylreste führt zum freien