Hydrazine/phenylhydrazine-mediated reductive dicarbonyl coupling reactions have been carried out under mild conditions to provide polycyclic aromatic compounds and azo-substituted polyaromatic compounds. This method has a broad substrate scope with good functional group compatibility.
Download full-text PDF |
Source |
|---|---|
| http://dx.doi.org/10.1039/d1ob02207e | DOI Listing |
Publication Analysis
Top Keywords
Similar Publications
Rediscovering Bacon's hydrazine/phenylhydrazine mediated cyclization of 2,2'-dicarbonylbi(hetero)aryls: construction of (5-azo)-/indazolo[2,3-]quinolines.
Org Biomol Chem
January 2022
Division of Organic Chemistry, CSIR-National Chemical Laboratory, Dr. Homi Bhabha Road, Pune 411 008, India.
Hydrazine/phenylhydrazine-mediated reductive dicarbonyl coupling reactions have been carried out under mild conditions to provide polycyclic aromatic compounds and azo-substituted polyaromatic compounds. This method has a broad substrate scope with good functional group compatibility.
View Article and Find Full Text PDFWant 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!