Synthesis of the Spider Toxins Nephilatoxin-9 and -11 by a Novel Solid-Phase Strategy
✍ Scribed by Bycroft, B. W.; Chan, W. C.; Hone, N. D.; Millington, S.; Nash, I. A.
- Book ID
- 126435948
- Publisher
- American Chemical Society
- Year
- 1994
- Tongue
- English
- Weight
- 225 KB
- Volume
- 116
- Category
- Article
- ISSN
- 0002-7863
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
The cyclic dehydrodepsipeptide, AM-toxin II, was efficiently synthesized by a solid-phase method using a novel selenyl linker. The cleavage from the resin with formation of a double bond is successfully achieved under mild oxidative conditions with TBHP.
## Abstract The first synthesis of a glycolipid library by hydrophobically assisted switching phase (HASP) synthesis is described. HASP synthesis enables flexible switching between solution‐phase steps and solid‐supported reactions conducted with molecules attached to a hydrophobic silica support.
## Abstract The incorporation of a specific cleavage site into an oligodeoxynucleotide can be achieved by utilizing the four 5′‐__S__‐(4,4′‐dimethoxytrityl)‐2′‐deoxy‐5′‐thionucleoside 3′‐(2‐cyanoethyl diisopropylphosphoramidites) **5** and **15a**–**c** (__Fig. 1__). Based on the silver ion assiste