The trisaccharide a-D-Manp-( l-+2)-a-D-Manp-(l-+2)-D-Man was synthesised by using a stepwise method. A key reaction in the preparation of the intermediates was the selective hydrogenolysis of mannopyranoside derivatives having both dioxane-and dioxolane-type benzylidene acetals, resulting in the exc
✦ LIBER ✦
Synthesis of O-β-d-mannopyranosyl-(1→4)-O-α-l-rhamnopyranosyl-(1→3)-d-galactopyranose, the trisaccharide repeating-unit of the O-specific polysaccharide from Salmonella anatum
✍ Scribed by N.K. Kochetkov; B.A. Dmitriev; N.N. Malysheva; A.Ya. Chernyak; E.M. Klimov; N.E. Bayramova; V.I. Torgov
- Book ID
- 108308834
- Publisher
- Elsevier Science
- Year
- 1975
- Tongue
- English
- Weight
- 639 KB
- Volume
- 45
- Category
- Article
- ISSN
- 0008-6215
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
Synthesis of O-α-d-mannopyranosyl-(1→2)-
✍
András Lipták; János Imre; Pál Nánási
📂
Article
📅
1983
🏛
Elsevier Science
🌐
English
⚖ 446 KB
Synthesis of bacterial antigenic polysac
✍
N. K. Kochetkov; B. A. Dmitriev; A. V. Nikolaev
📂
Article
📅
1977
🏛
Springer
🌐
English
⚖ 361 KB
Anomalous Zemplén deacylation reactions
✍
Zoltán Szurmai; András Lipták; Günther Snatzke
📂
Article
📅
1990
🏛
Elsevier Science
🌐
English
⚖ 476 KB
The crystal and molecular structure of O
✍
Vincent Warin; Frano̧cois Baert; René Fouret; Gérard Strecker; Geneviève Spik; B
📂
Article
📅
1979
🏛
Elsevier Science
🌐
English
⚖ 664 KB
The crystal structure of a-D-Manp-(1 +3)-/?-D-Manp-( 1-+4)-a-D-GlcNAcp has been determined by the direct method using the multi-solution, tangentzformula, and "magic integer" procedures. The space group is P2,, and 2 molecules are in the unit cell with c1 = 9.894 ( 5), b = 10.372 (6), c = 11.816 (6)
Synthesis of propyl O-(α-L-rhamnopyranos
✍
Lu Shou-F'U; Ouyang Qin-Qin; Guo Zhong-Wu; W Biao; Hui Yong-Zheng
📂
Article
📅
2010
🏛
John Wiley and Sons
🌐
English
⚖ 635 KB
Synthesis of the principal chain of the
✍
N. É. Bairamova; L. V. Bakinovskii; N. K. Kochetkov
📂
Article
📅
1985
🏛
Springer
🌐
English
⚖ 655 KB