Sulfur-containing spirocyclic compounds based on 3-methyl-(amino)-1-phenylpyrazol-5-ones
โ Scribed by Yu. G. Shermolovich; S. V. Emets
- Book ID
- 105525600
- Publisher
- Springer US
- Year
- 2000
- Tongue
- English
- Weight
- 230 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0009-3122
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
composition, and IR spectrumi3] with the product prepared from SOClz and HzS,. This new, more productive synthetic route requires much less time and experimental effort than the former preparation. ## Procedtwe: Sg (3.76g, 14.7mmol)isdissolved in CHzC12 (800ml) by refluxing. The homogeneous soluti
Reaction of 5-Azacytosine with 3-Methyl-1-phenylpyrazol-5-one. -The first example of the reaction of 5-azacytosine (I) with an uncharged C-nucleophile is presented. The title reaction proceeds with destruction of the 5-azacytosine cycle to afford the dipyrazolylmethane (III). This compound is also