The amination step involves introducing an amino group (NH2) at the desired position on the alkene. This step is crucial for the regioselective formation of the pyrrolone ring. The amino group typically attacks the alkene to form a C-N bond, leading to the desired pyrrolone intermediate.
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2-Decenoic acid, 4-(butylamino)-, methyl ester, (E)-
Benzamide, N-(2-iodophenyl)-N-methyl-
(S)-tert-butyl (1-phenyloctan-2-yl)carbamate
2-methyl-6-(4-nitrophenyl)imidazo[2,1-b][1,3,4]thiadiazole
