Click chemistry reactions in medicinal chemistry: Applications of the 1,3‐dipolar cycloaddition between azides and alkynes
Università degli Studi del Piemonte Orientale “Amedeo Avogadro” · Probiotical (Italy)
Abstract
In recent years, there has been an ever-increasing need for rapid reactions that meet the three main criteria of an ideal synthesis: efficiency, versatility, and selectivity. Such reactions would allow medicinal chemistry to keep pace with the multitude of information derived from modern biological screening techniques. The present review describes one of these reactions, the 1,3-dipolar cycloaddition ("click-reaction") between azides and alkynes catalyzed by copper (I) salts. The simplicity of this reaction and the ease of purification of the resulting products have opened new opportunities in generating vast arrays of compounds with biological potential. The present review will outline the accomplishments of…
Citation impact
- FWCI
- 19.74
- Percentile
- 100%
- References
- 130
Authors
6- GCGian Cesare TronCorresponding
Università degli Studi del Piemonte Orientale “Amedeo Avogadro”, Probiotical (Italy)
- TPTracey Pirali
Università degli Studi del Piemonte Orientale “Amedeo Avogadro”, Probiotical (Italy)
- RBRichard Billington
Università degli Studi del Piemonte Orientale “Amedeo Avogadro”, Probiotical (Italy)
- PLPier Luigi Canonico
Università degli Studi del Piemonte Orientale “Amedeo Avogadro”, Probiotical (Italy)
- GSGiovanni Sorba
Università degli Studi del Piemonte Orientale “Amedeo Avogadro”, Probiotical (Italy)
Topics & keywords
- Click chemistry
- Cycloaddition
- Chemistry
- Combinatorial chemistry
- Nanotechnology
- Organic chemistry
- Computer science
- Catalysis