5-Heteroarylthymine analogs (5) were synthesized via binucleophilic attack with bidentate thiols on the cyano group of cyanoacetylurea to form the heteroarylurea derivatives (2-4) followed by their cyclization with formamide. Also, their nucleosides 6a and 6b with 2,3,4,6-tetra-O-acetyl-β£-D-glucopyr
ChemInform Abstract: Activated Nitriles in Heterocyclic Synthesis: Facile Synthesis of Heteroarylthymine Analogues and Their Nucleosides.
β Scribed by Yehia A. Allam; Laila M. Chabaka; Galal A. M. Nawwar
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 32 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v