Journal
APPLIED ORGANOMETALLIC CHEMISTRY
Volume 36, Issue 5, Pages -Publisher
WILEY
DOI: 10.1002/aoc.6664
Keywords
1; 2; 3-triazole; antifungal agents; click chemistry; CuMCs; molecular docking
Categories
Funding
- Directorate of Minorities, Government of Karnataka, Bengaluru
- Vision Group on Science and Technology, Government of Karnataka, Bangalore [567/2016-17/2020-21/47]
- KsST
Ask authors/readers for more resources
A green and efficient method for the synthesis of 1,2,3-triazoles was developed using click chemistry on copper microcrystals. The method showed short reaction times, high yields, and excellent purity, with a catalyst that is environmentally friendly. The synthesized compounds exhibited promising antifungal activity.
A remarkable, efficacious, and environmental friendly one-pot procedure affianced for the synthesis of 1,2,3-triazoles by 1,3-dipolar cycloaddition of aromatic azides, terminal alkynes over Cu microcrystals (CuMCs) by click chemistry as subsequent way. The predominance of this method is green synthetic pathway, transient reaction times, facile workup, exceptional yields (87% to 90%) with excellent purity, regioselective single product formation, and eco-friendliness of the CuMCs catalyst. Docking studies manifested strong binding interactions with enzyme sterol 14-alpha-demethylase (PDB ID: 3KHM) with excellent C-score values. The antifungal screening of synthesized compounds revealed promising activity.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available