A synthetic strategy has been developed for the synthesis of 1-azaanthraquinones. This synthetic protocol consists of sequential Pd-catalyzed carbon-nitrogen bond formation followed by Lewis acid catalyzed intramolecular cyclization. The Pd-catalyzed aminated intermediate was isolated and characterized. This sequential reactions strategy provides a wide range of 1-azaanthraquinones with good yields.
Download full-text PDF |
Source |
|---|---|
| http://dx.doi.org/10.1021/acs.joc.7b01427 | DOI Listing |
Publication Analysis
Top Keywords
acid catalyzed
8
catalyzed intramolecular
8
intramolecular cyclization
8
synthesis 1-azaanthraquinone
4
1-azaanthraquinone sequential
4
sequential c-n
4
c-n bond
4
bond formation/lewis
4
formation/lewis acid
4
cyclization strategy
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!