Govindaraju, M. and Vasanth Kumar, G. and Ajay, K. (2014) Synthesis and antimicrobial activity of novel isoxazolines by 1, 3-dipolar cycloaddition reactions. International Journal of ChemTech Research, 6 (2). pp. 886-890. ISSN 0974-4290
Full text not available from this repository. (Request a copy)
Official URL: http://sphinxsai.com/2014/CTVOL6/CT=02(886-890)AJ1...
Abstract
Nitrile oxides were generated by the catalytic dehydrogenation of aromatic aldehyde oximes 2a-g with chloramine-T as oxidizing agent. The 1,3-dipolar cycloaddition of in situ generated nitrile oxides with ethyl oleate 1 produced a series of new ethyl 8-(3-aryl-4-octyl-4,5-dihydroisoxazol-5-yl)octanoate 3a-g in 65- 84 yield. Some of the synthesized cycloadducts have exhibited moderate to good antifungal and antibacterial activity.
| Item Type: | Article |
|---|---|
| Uncontrolled Keywords: | Cycloaddition and Dipolar and Isoxazolines and Antifungal and Antibacterial and MIC's. |
| Subjects: | C Chemical Science > Chemistry |
| Divisions: | Yuvaraj college > Chemistry |
| Depositing User: | Users 19 not found. |
| Date Deposited: | 18 Oct 2019 09:54 |
| Last Modified: | 16 Jul 2022 07:05 |
| URI: | http://eprints.uni-mysore.ac.in/id/eprint/9290 |
Actions (login required)
 |
View Item |
