Copper-Catalyzed Azide–Alkyne Cycloaddition: Regioselective Synthesis of 1,4,5-Trisubstituted 1,2,3-Triazoles
✍ Scribed by Christian Spiteri; John E. Moses
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 227 KB
- Volume
- 49
- Category
- Article
- ISSN
- 0044-8249
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📜 SIMILAR VOLUMES
on the occasion of his 60th birthday The development of functionnalized organometallic compounds is a dramatically growing field, and considerably broadens the scope of these nucleophilic reagents. [1] An important breakthrough in the preparation of these reactive species, which contain sensitive f
Triazoles bearing the appropriate substituents at the 4-and 5-positions can rearran-An interesting application was found re-ge thermally via open-chain diazoirnine intermediates. cently in the transformation of l-phenyl-l,2,3-triazole-4-carbaldehyde into l-alkyl-l,2, 3-triazole-4-carbaldehydes throu
and 3-aminopyrazole and 3-amino-1,2,4-triazole provide convenient access to biologically relevant 3H-imidazo[1,2-b]pyrazoles and a 5H-imidazo[2,1-c][1,2,4]triazole.