Synthesis of a Puromycin Analog
β Scribed by Doz. Dr. F. W. Lichtenthaler; Dr. H. P. Albrecht
- Publisher
- John Wiley and Sons
- Year
- 1968
- Tongue
- English
- Weight
- 215 KB
- Volume
- 7
- Category
- Article
- ISSN
- 0044-8249
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
The synthesis of a new carbocyclic nucleoside starting from aucubin, a natural methylcyclopentanoid monoterpene, has been performed, allowing the preparation of aucubovir II, a carbocyclic nucleoside analog with a highly functionalized
Dynemicin A is a member of the family of enediyne natural the enediyne, and the oxirane ring but lack the nitrogen heterocycle. In these compounds the aryl ring assumes a products. It is unique in that it combines a ten-membered enediyne with an anthraquinone substructure. These different conformati