AI Article Synopsis
- - The study focuses on synthesizing 3-benzoylisoxazolines by reacting alkenes with various α-nitroketones using chloramine-T as the base.
- - It explores a wide range of α-nitroketones and alkenes, resulting in the formation of different isoxazolines and isoxazoles.
- - Chloramine-T is highlighted as a cost-effective and user-friendly moderate base for facilitating the 1,3-dipolar cycloaddition reaction.
Article Abstract
In this study, 3-benzoylisoxazolines were synthesized by reacting alkenes with various α-nitroketones using chloramine-T as the base. The scope of α-nitroketones and alkenes is extensive, including different alkenes and alkynes to form various isoxazolines and isoxazoles. The use of chloramine-T, as the low-cost, easily handled, moderate base for 1,3-dipolar cycloaddition is attractive.
Download full-text PDF |
Source |
|---|---|
| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8227129 | PMC |
| http://dx.doi.org/10.3390/molecules26123491 | DOI Listing |
Publication Analysis
Top Keywords
13-dipolar cycloaddition
8
3-benzoylisoxazolines 13-dipolar
4
cycloaddition chloramine-t-catalyzed
4
chloramine-t-catalyzed condensation
4
condensation α-nitroketones
4
α-nitroketones dipolarophiles
4
dipolarophiles study
4
study 3-benzoylisoxazolines
4
3-benzoylisoxazolines synthesized
4
synthesized reacting
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!