A ready asymmetric synthesis of 3Ј-oxathionucleosides has overall yield and considerable enantiomeric excesses. It represents a general synthetic path to prepare a wide range been accomplished in three main steps from benzoyloxyethanal. The synthesis is characterized by high of heterosubstituted sul
Design, Synthesis and Cytotoxicity of a New Series of Isoxazolidine Based Nucleoside Analogues
✍ Scribed by Dorota G. Piotrowska; Marcin Cieślak; Karolina Królewska; Andrzej E. Wróblewski
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- English
- Weight
- 208 KB
- Volume
- 344
- Category
- Article
- ISSN
- 0365-6233
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract Thirty genistein (=5,7‐dihydroxy‐3‐(4‐hydroxyphenyl)‐4__H__‐1‐benzopyran‐4‐one; GEN) derivatives were synthesized from genistein through a facile approach in high yields. Compounds **9, 11, 12, 23**–**30** were reported for the first time, while **13**–**22** have already been reported
A total of 17 resveratrol ( ¼ (E)-5-[2-(4-hydroxyphenyl)ethenyl]benzene-1,3-diol) derivatives were synthesized from resveratrol (RES) through a facile approach. Among them, 13 compounds, 2 and 6 -17, were reported for the first time, while 1 and 3 -5 had already been reported several years ago. The