𝔖 Bobbio Scriptorium
✦   LIBER   ✦

The synthesis of trideoxy sugars. A preparation of rhodinose (2,3,6-trideoxy-L-threo-hexose) and methyl 2,3,6-trideoxy-α-L-erythro-hexopyranoside

✍ Scribed by A.H. Haines


Book ID
108307957
Publisher
Elsevier Science
Year
1972
Tongue
English
Weight
898 KB
Volume
21
Category
Article
ISSN
0008-6215

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Syntheses of methyl 2,6-diacetamido-2,3,
✍ Mohammed M. Abuaan; John S. Brimacombe; Leslie C.N. Tucker 📂 Article 📅 1984 🏛 Elsevier Science 🌐 English ⚖ 612 KB

The title glycosides were synthesised from D-glUCOSe, via the common intermediate methyl 2-acetamido-4-O-benzoyld-bromo-2,3,6-trideoxy-a-D-ribohexopyranoside . \*To whom enquiries should be addressed. \*\*The overall efficiency of this procedure can be improved by using a phase-transfer process' in

The synthesis of a derivative of l-decil
✍ John S. Brimacombe; Khandker M.M. Rahman 📂 Article 📅 1985 🏛 Elsevier Science 🌐 English ⚖ 261 KB

L-Decilonitrose2 (1, 2,3,6-trideoxy-3-C-methyl-3-nitro-L-ribo-hexose) is the latest methyl-branched nitro sugar to be found as an antibiotic component. Other members of this novel group of sugars are L-evernitrose3 (2, from the evernino-micins4), D-rubranitrose5 (3, from rubradirin6), and D-kijanos