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Stereoselective Synthesis of Cannabidiol and its Unnatural Enantiomer to Evaluate Anxiolytic‐Like Properties and Memory Interactions

24.07.2025
Stereoselective Synthesis of Cannabidiol and its Unnatural Enantiomer to Evaluate Anxiolytic‐Like Properties and Memory Interactions

Von Wiley-VCH zur Verfügung gestellt

Both (−)- and (+)-cannabidiol (CBD and ent-CBD, respectively) are synthesized via a highly diastereoselective CSA-catalyzed Friedel–Crafts reaction. ent-CBD exhibits anxiolytic-like effects in aged male mice without impairing long-term memory formation.


(−)-Cannabidiol (CBD) is a nonpsychotropic phytocannabinoid found in Cannabis strains with well-established pharmacological applications. Conversely, (+)-cannabidiol (ent-CBD), the non-natural enantiomer of CBD, has been involved in a limited number of pharmacological studies. Therefore, CBD and ent-CBD are synthesized using (R)-(−)- and (S)-(+)-carvone as starting materials, respectively, via a highly diastereoselective 10-camphorsulfonic acid (CSA) catalyzed Friedel–Crafts reaction as the key step. Pharmacological studies are conducted using the plus-maze discriminative avoidance task (PM-DAT) to evaluate the interaction between memory and anxiety-like behavior as well as spontaneous motor activity in both young adult and aged male mice. The results show that ent-CBD at a dose of 20 mg kg−1 has an anxiolytic-like effect in aged male mice. In addition, ent-CBD did not impair discriminative avoidance memory formation at all doses evaluated.

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