“…[3][4][5][6] Thus, it can serve as a precursor for the development of new botanical fungicide. Moreover, among the family of fivemembered nitrogen/oxygen-containing aromatic heterocycles, 1,3,4-oxadiazole and 1,2,4-triazole scaffolds are widely present in pharmaceutical or pesticide molecules, and exhibited a pronounced diversity of biological activities due to their ability to form interactions with various enzymes, proteins, and receptors in organisms, [7][8][9] such as anticancer, [10,11] antiviral, [12,13] antibacterial, [14][15][16] antifungal, [17][18][19] and herbicidal [20] activities (Figure 1). It is well known that molecular hybridization and diversity-oriented synthesis (DOS) approach are powerful strategies for constructing diverse highly active molecular structures, we wondered if we could obtain novel fungicide with excellent biological activity and specific mechanisms of action by fusing 1,3,4-oxadiazole and 1,2,4-triazole rings with phthalide skeleton according to the principle of bioactive substructure combination.…”