## Abstract Mannose (α‐Man)‐containing neoglycoconjugates possessing aliphatic‐, aromatic‐, and carbohydrate‐centered architectures and differing in structural characteristics such as valency, topology, and nature of the linker have been synthesized using click chemistry that shows its value as an
Stereocontrolled syntheses of phorbol analogs and evaluation of their binding affinity to PKC
✍ Scribed by Kazuyuki Sugita; Charles F. Neville; Mikiko Sodeoka; Hiroaki Sasai; Masakatsu Shibasaki
- Book ID
- 103402177
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- French
- Weight
- 227 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0040-4039
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📜 SIMILAR VOLUMES
An improved, high yield procedure for the ester enolate Claisen rearrangement of 2-butenyl fluoroacetate to form stereoselectively 2-fluoro-3-methylpent-4-enoic-y acid (1) will be reported. The conversion of the acids (1) to 2-fluoro-3-methyl-r
## Abstract __Wittig__ olefination of (2__S__,3__R__,5__S__,6__R__)‐5‐(acetyloxy)‐tetrahydro‐6‐[(methoxymethoxy)methyl]‐3‐(phenylthio)‐ 2__H__‐pyran‐2‐acetaldehyde ((+)‐**10**) with {2‐[(2__S__,3__R__,4__R__,5__R__,6__S__)‐tetrahydro‐3,4,5‐tris(methoxymethoxy)‐6‐methyl‐ 2__H__‐pyran‐2‐yl]ethyl}trip