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- W4376504384 abstract "The 2-cyano-3-(indol-3-yl)acryloyl chloride, a building block synthon prepared in good yield, was utilized for the synthesis of various indolylacrylamide and indole-based heterocycles. Thus, the aforementioned acid chloride was allowed to react with various oxygen, sulfur, and nitrogen nucleophiles, in addition to mono- and bidentate nucleophiles. The pyrazolidine derivatives were produced on interactions with phenylhydrazine and 2-cyanoethanohydrazide. The antioxidant activity of the synthesized compounds was assessed using the phosphomolybdenum technique and ascorbic acid as a standard. The findings displayed that indolyl-based azine, pyrazolidine, cyanoacetamide, and benzodiazepine derivatives were the most active antioxidants." @default.
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- W4376504384 date "2023-05-13" @default.
- W4376504384 modified "2023-09-27" @default.
- W4376504384 title "Facile Synthesis and Antioxidant Activity Screening of Some Novel 3-Substituted Indole Derivatives" @default.
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- W4376504384 doi "https://doi.org/10.1080/10406638.2023.2210729" @default.
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