4.1 Article

Laccase-catalysed azide-alkyne cycloadditions: Synthesis of benzothiazole and benzimidazole fused 1,2,3-triazole derivatives by copper containing oxidoreductase enzymes

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TAYLOR & FRANCIS LTD
DOI: 10.1080/10242422.2022.2140588

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Biocatalysis; click chemistry; enzyme; laccase

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A new method for synthesizing triazole rings was proposed using laccase-catalyzed reactions. Through the reaction of benzothiazoles and benzimidazoles-functionalized alkynes with aryl azides, 1,2,3-triazole-fused products were obtained.
A new approach for synthesizing triazole rings through the application of laccases, copper containing oxidoreductase enzymes is outlined. A series of benzothiazoles and benzimidazoles-functionalized alkynes were initially synthesized utilizing a biocatalysis laccase-based approach. The resultant alkynes were further treated with aryl azides in a 1,3-dipolar cycloaddition reaction facilitated by laccase enzymes to obtain 1,2,3-triazole-fused benzothiazoles and benzimidazoles.

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