The term "asymmetric" in organic chemistry typically refers to reactions that produce chiral products, meaning the products have a specific three-dimensional arrangement of atoms that are not superimposable on their mirror images. Asymmetric reactions are often catalyzed by chiral catalysts, which selectively promote the formation of one enantiomer (mirror-image isomer) over the other. This is important in the synthesis of complex molecules with defined stereochemistry.
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2-hydroxy-4-(4-methoxy-phenyl)-2-trifluoromethyl-pent-4-enoic acid ethyl ester
1H-Isoindole-1,3(2H)-dione, 2-[3-(4-fluorophenyl)-2-propenyl]-, (E)-
3-(3,4-dichlorophenyl)-3-oxo-1-propanol
Phentydrone
imidazole
