| Autor: |
Yadagiri D; Department of Chemistry and Biochemistry, University of Texas at Dallas, 800 West Campbell Road, Richardson, Texas 75080-3021, United States., Rivas M; Department of Chemistry and Biochemistry, University of Texas at Dallas, 800 West Campbell Road, Richardson, Texas 75080-3021, United States., Gevorgyan V; Department of Chemistry and Biochemistry, University of Texas at Dallas, 800 West Campbell Road, Richardson, Texas 75080-3021, United States. |
| Abstrakt: |
The high demand for new and efficient routes toward synthesis of nitrogen-containing heterocyclic scaffolds has inspired organic chemists to discover several methodologies over recent years. This Perspective highlights one standout approach, which involves the use of pyridotriazoles and related compounds in denitrogenative transformations. Readily available pyridotriazoles undergo ring-chain isomerization to produce uniquely reactive α-diazoimines. Such reactivity, enabled by metal catalysts, additives, or visible-light irradiation, can be applied in transannulation, insertion, cyclopropanation, and many other transformations. |
