The core trisacchande common to all asp~ragine-linked glycopmtein oligosaccharides was synthesized using two novel processes: I) regioselective acetylation using lipase, and 2) inversion of the C-2 hydroxyl group of the glucose residue in a glucosyl chitobiose derivative to produce the corresponding
β¦ LIBER β¦
A new strategy for the synthesis of the nephritogenoside trisaccharide unit using phenylsulfenyl donors
β Scribed by Hong Zhang; Yali Wang; Wolfgang Voelter
- Book ID
- 103402208
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- French
- Weight
- 238 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
A new strategy for the synthesis of the
β
Ichiro Matsuo; Megumi Isomura; Richard Walton; Katsumi Ajisaka
π
Article
π
1996
π
Elsevier Science
π
French
β 208 KB
A new strategy for the synthesis of Asp-
A new strategy for the synthesis of Asp-Gly units-containing glycopeptides using Fmoc/Bzl protection
β
Hong Mang; Yali Wang; Wolfgang Voelter
π
Article
π
1995
π
Elsevier Science
π
French
β 362 KB
A New Strategy for the Synthesis of Poly
β
Ye-Zi You; Chun-Yan Hong; Cai-Yuan Pan
π
Article
π
2002
π
John Wiley and Sons
π
English
β 594 KB
A new strategy for the synthesis of unsy
β
Hu Jun; Ding Yi-Xiang
π
Article
π
2010
π
John Wiley and Sons
π
English
β 256 KB
π 2 views
A versatile new strategy for the synthes
β
Martin G. Banwell; RenΓ© Onrust
π
Article
π
1985
π
Elsevier Science
π
French
β 209 KB
Pi= Swern-type oxidation of various 7-halogenobicyclo[4.l.O]heptane-2,3-or -3,4- 10 s affords the corresponding bicyclic diketones which undergo in situ ring expansion and loss of hydrogen halide to give a-tropolones in high yieme quantitative conversion of the isolable 1,4-diketone 26 into the y-tr
A new strategy for the stereoselective s
β
Piotr Dybowski; Aleksandra SkowroΕska
π
Article
π
1991
π
Elsevier Science
π
French
β 191 KB