| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5258847 | Tetrahedron Letters | 2016 | 8 Pages |
Abstract
A tunable approach to the oxidative and eliminative cycloadditions of nitroolefins with organic azides are demonstrated under solvent free condition. A series of 1,5-disubstituted-1,2,3-triazoles with/without nitro group have been synthesized from moderate to excellent yields.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
![A tunable route to oxidative and eliminative [3+2] cycloadditions of organic azides with nitroolefins: CuO nanoparticles catalyzed synthesis of 1,2,3-triazoles under solvent-free condition](/preview/png/5258847.png "First Page Preview: A tunable route to oxidative and eliminative [3+2] cycloadditions of organic azides with nitroolefins: CuO nanoparticles catalyzed synthesis of 1,2,3-triazoles under solvent-free condition")
Authors
D. Gangaprasad, J. Paul Raj, T. Kiranmye, R. Sasikala, K. Karthikeyan, S. Kutti Rani, J. Elangovan,