Abstract
A novel regioselective route to 1-aryl-4-bromo-5-trifluoromethylpyrazoles involves reactions of arylhydrazines with 3-bromo-4-ethoxy-1,1,1-trifluorobut-3- en-2-one.
| Original language | English |
|---|---|
| Pages (from-to) | 172-173 |
| Number of pages | 2 |
| Journal | Russian Chemical Bulletin |
| Volume | 55 |
| Issue number | 1 |
| DOIs | |
| Publication status | Published - Jan 2006 |
| MoE publication type | A1 Journal article-refereed |
Funding
This work was financially supported by the Russian Science Support Foundation.
Keywords
- Arylhydrazines
- Enones
- Heterocyclization
- Organofluorine compounds
- Pyrazoles
Fingerprint
Dive into the research topics of 'Regioselective synthesis of 1-aryl-4-bromo-5-trifluoromethylpyrazoles'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver