𝔖 Bobbio Scriptorium
✦   LIBER   ✦

The use of positively charged leaving-groups in the synthesis of α-D-linked glucosides. Synthesis of methyl 2,3,4-tri-O-benzyl-6-O-(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-α-D-glucopyranoside

✍ Scribed by Ronald Eby; Conrad Schuerch


Book ID
108308187
Publisher
Elsevier Science
Year
1975
Tongue
English
Weight
426 KB
Volume
39
Category
Article
ISSN
0008-6215

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


One-pot synthesis of 1-allyl- and 1-alle
✍ Shang-Cheng Hung; Chun-Cheng Lin; Chi-Huey Wong 📂 Article 📅 1997 🏛 Elsevier Science 🌐 French ⚖ 180 KB

A one-pot synthesis of 1-allyl-and 1-allenyl-6-O-acetyl-2,3,4-tri-O-benzyl-ot-D-glycosides from the corresponding methyl per-benzyl-tx-D-glycosides and allyl trimethylsilane or propargyl trimethylsilane in the presence of trimethylsilyl trifluoromethanesulfonate followed by addition of acetic anhydr

Synthesis of allyl and benzyl 4-O-(3,6-d
✍ Jose R. Mariño-Albernas; Vicente Verez-Bencomo; Leandro Gonzalez; Carlos S. Pere 📂 Article 📅 1987 🏛 Elsevier Science 🌐 English ⚖ 803 KB

Condensation of 2,4-di-O-acetyl-3,6-di-O-methyl-a-~glucopyranosyl bromide with either ally1 or benxyl2,4-di-0-methyl-cu+rhamnopyranoside in the presence of mercuric cyanide, followed by 0-deacetylation, gave the title oligosaccharides in excellent yields.