Baylis-Hillman reactions of 2-nitrobenzaldehydes with various activated alkenes afford adducts that undergo reductive cyclisation to quinoline derivatives. The chemo- and regioselectivity of cyclisation appears to be influenced by the choice of both the substrate and the reagent system, and competing reactions have been observed.
Download full-text PDF |
Source |
|---|---|
| http://dx.doi.org/10.1039/b608592j | DOI Listing |
Publication Analysis
Top Keywords
quinoline derivatives
8
baylis-hillman approach
4
approach quinoline
4
derivatives baylis-hillman
4
baylis-hillman reactions
4
reactions 2-nitrobenzaldehydes
4
2-nitrobenzaldehydes activated
4
activated alkenes
4
alkenes afford
4
afford adducts
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!