𝔖 Bobbio Scriptorium
✦   LIBER   ✦

The path of the conversion of 3,5,6-tri-O-benzoyl-1,2-O-isopropylidene-?-D-glucose into 4,5,6-tri-O-benzoyl-2,3-di-S-ethyl-2,3-dithio-D-allose diethyl dithioacetal

✍ Scribed by Bethell, G. S.; Ferrier, R. J.

Book ID
118137320
Publisher
Royal Society of Chemistry
Year
1972
Weight
695 KB
Volume
0
Category
Article
ISSN
1472-7781

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Synthesis of 1,6-anhydro-2,3-di-O-benzoy
Synthesis of 1,6-anhydro-2,3-di-O-benzoyl-4-O-(methyl 2,3,4-tri- O-benzoyl-Ξ±-l-idopyranosyluronate)-Ξ²-d-glucopyranose from cellobiose
✍ Yoshitaka Ichikawa; Hiroyoshi Kuzuhara πŸ“‚ Article πŸ“… 1983 πŸ› Elsevier Science 🌐 English βš– 986 KB

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