preparation of methyl 3,6-dideoxy-D-xylo-hexapyranoside (methyl abequoside) having deuterium stereospecifically labeled at the 3s (1) and 3R (2) position, respectively, via three different routes is described. The 3.6~didwxyhexoses are found in the lipopolysaccharides of a number of gram-negative b
✦ LIBER ✦
Synthesis of stereospecifically labeled carbohydrates: Preparation of (3S)− and (3R)-[3-2H1]ascarylose
✍ Scribed by Oksoo Han; Hung-wen Liu
- Publisher
- Elsevier Science
- Year
- 1987
- Tongue
- French
- Weight
- 213 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
Synthesis of stereospecifically labeled
✍
Theresa M. Weigel; Hung-wen Liu
📂
Article
📅
1988
🏛
Elsevier Science
🌐
French
⚖ 240 KB
The stereospecific synthesis of (2S,3R)
✍
Jack E. Baldwin; Robert M. Adlington; David W. Gollins; Christopher R.A. Godfrey
📂
Article
📅
1995
🏛
Elsevier Science
🌐
French
⚖ 632 KB
Synthesis of (2S,2′R,3′R)-2-(1′-[3H],2′,
✍
Jürgen Wichmann; Philipp Huguenin; Geo Adam
📂
Article
📅
2000
🏛
John Wiley and Sons
🌐
French
⚖ 248 KB
👁 1 views
Experiments with stereospecifically-labe
✍
U. Müller; D.H.G. Crout
📂
Article
📅
1975
🏛
Elsevier Science
🌐
English
⚖ 264 KB
Preparation of 2H- and 3H-labelled carvo
✍
Derek V. Banthorpe; Geoffrey D. Brown
📂
Article
📅
1989
🏛
John Wiley and Sons
🌐
French
⚖ 240 KB
The first, involving a reversible ene reaction yielded 10-deuteriocarvone with some substitution at other reactive centres, An improverent to this route involved the decomposition of an organozinc reagent of 10-chlorocarvone which gave a better yield of product substituted only at C-10, As a prelini
Stereospecific preparation of glycidic e
✍
Odile Cabon; Didier Buisson; Marc Larcheveque; Robert Azerad
📂
Article
📅
1995
🏛
Elsevier Science
🌐
English
⚖ 521 KB