[Reaction: see text]. An efficient highly regioselective protocol for the synthesis of isomeric 1,3-diaryl (or 1-aryl-3-alkyl) and 1,5-diaryl (or 1-aryl-5-alkyl)-5 (or 3)-(N-cycloamino)pyrazoles has been reported by cyclocondensation of common alpha-oxoketene N,S-acetal precursors with arylhydrazines by variation of reaction conditions.
Download full-text PDF |
Source |
|---|---|
| http://dx.doi.org/10.1021/jo051478u | DOI Listing |
Publication Analysis
Top Keywords
highly regioselective
8
regioselective synthesis
4
synthesis 1-aryl-3
4
1-aryl-3 5-alkyl/aryl-5
4
5-alkyl/aryl-5 3-n-cycloaminopyrazoles
4
3-n-cycloaminopyrazoles [reaction
4
[reaction text]
4
text] efficient
4
efficient highly
4
regioselective protocol
4
Similar Publications
Want AI Summaries of new PubMed Abstracts delivered to your In-box?
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!