Depending on the reaction conditions and the structure of the azole, control over stereochemistry can be achieved. This is particularly important when synthesizing chiral compounds with specific biological activities.
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nonyl(phenyl)sulfane
3-methyl-2-phenylquinoline-4-carbonyl chloride
C66H69N5O19
1H-Imidazole-4-carboxylic acid, 1-(phenylmethyl)-, methyl ester
3-Pentanone, 5-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-1-hydroxy-4-methyl-1-phenyl-, (1R,4S)-
