𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Formation of β-1,4-Oligoglucosides by Certain Acetobacter Species

✍ Scribed by STEEL, ROBERT; WALKER, THOMAS K.

Book ID
109593996
Publisher
Nature Publishing Group
Year
1957
Tongue
English
Weight
222 KB
Volume
180
Category
Article
ISSN
0028-0836

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A highly stereoselective β-(1→4)-glycosi
A highly stereoselective β-(1→4)-glycosidic bond formation by reductive cleavage of cyclic orthoesters
✍ Takamasa Iimori; Hiro Ohtake; Shiro Ikegami 📂 Article 📅 1997 🏛 Elsevier Science 🌐 French ⚖ 230 KB

Sterically congested glycosides, glycosyl-13-(1--->4)-glycosides, were stereoselectively synthesized by reduction of glycosidic spiro-orthoesters with LiAIH4-AICI3. This novel transformation is especially valuable when it is applied to the preparation of mannosyl-13-(1--->4)-glycoside which must be

The Formation of Bridged Bicyclic 1,2,4-
The Formation of Bridged Bicyclic 1,2,4-Trioxanes by Intramolecular Capture of β-Hydroperoxy Cations
✍ Charles W. Jefford; France Favarger; Serenella Ferro; Daniel Chambaz; Alain Brin 📂 Article 📅 1986 🏛 John Wiley and Sons 🌐 German ⚖ 533 KB

The 1 ,I-endoperoxide, prepared from 3-(4-methylnaphth-1 -yl)propanal by photo-oxygenation in CH2C12, gave on treatment with Ambrrlyst-15 m, 3,3,4a,pyran in 85% yield. Its structure was determined by X-ray crystal structure analysis. The 1,2,4-trioxane moiety is locked in a twist-boat conformation w