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In this paper, the syntheses of twelve asymmetric curcumin analogs using Pabon’s method are reported. Generally, the previously reported yields of asymmetric curcuminoids, such as <b>9a</b> (53%), <b>9c</b> (38%), and <b>9k</b> (38%), have been moderate or low. Herein, we propose that the low yields were due to the presence of water and <i>n</i>-BuNH₂ in the reaction media. To prove this formulated hypothesis, we have demonstrated that the yields can be improved by adding molecular sieves (MS) (4 Å) to the reaction mixture, thus reducing the interference of water. Therefore, improved yields (41–76%) were obtained, except for <b>9b</b> (36.7%), <b>9g</b> (34%), and <b>9l</b> (39.5%). Furthermore, compounds <b>9b</b>, <b>9d</b>, <b>9e</b>, <b>9f</b>, <b>9g</b>, <b>9h</b>, <b>9i</b>, <b>9j</b>, and <b>9l</b> are reported herein for the first time. The structures of these synthetic compounds were determined by spectroscopic and mass spectrometry analyses. The free radical scavenging ability of these synthetic asymmetric curcuminoids was evaluated and compared to that of the positive control butylated hydroxytoluene (BHT). Among the synthesized asymmetric curcuminoids, compounds <b>9a</b> (IC₅₀ = 37.57 ± 0.89 μM) and <b>9e</b> (IC₅₀ = 37.17 ± 1.76 μM) possessed effective 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical scavenging abilities, and compounds <b>9h</b> (IC₅₀ = 11.36 ± 0.65 μM) and <b>9i</b> (IC₅₀ = 10.91 ± 0.77 μM) displayed potent 2,2’-azinobis-(3-ethylbenzthiazoline-6-sulphonate) (ABTS) radical scavenging abilities comparable to that of curcumin (IC₅₀ = 10.14 ± 1.04 μM). Furthermore, all the synthetic asymmetric curcuminoids were more active than BHT.