This search combines search strings from the content search (i.e. "Full Text", "Author", "Title", "Abstract", or "Keywords") with "Article Type" and "Publication Date Range" using the AND operator.
Beilstein J. Org. Chem. 2011, 7, 668–677, doi:10.3762/bjoc.7.79
Graphical Abstract
Figure 1: Isomeric forms of triazole.
Scheme 1: Copper catalyzed azide–alkyne cycloaddition.
Scheme 2: Ruthenium catalyzed azide–alkyne cycloaddition.
Scheme 3: Copper-sulfate catalyzed azide–alkyne cycloaddition.
Scheme 4: Azide–dimethylbut-2-yne-dioate cycloaddition.
Figure 2: Triazole compound 3 with most potent antifugal activity against various strains [20].
Figure 3: Triazole compounds 4 and 5 showing antifungal activity against Candida albicans [31].
Figure 4: Triazole compound 6 with the highest activity against Aspergillus flavus, Aspergillus versicolor, A...
Figure 5: Triazole compound 7 exhibiting an MIC of 25 µg/mL against Aspergillus niger [33].
Figure 6: Triazole compound 8 showing the most significant activity against Aspergillus niger and Fusarium ox...
Figure 7: Ergosterol biosynthesis inhibitor pathway.
Figure 8: Fluconazole (9).
Figure 9: Itraconazole (10).
Figure 10: Voriconazole (11).
Figure 11: Posaconazole (12).
Figure 12: Ravuconazole (13).