Electrochemically driven reductive cyclization of <i>o</i> -nitroanilines: synthesis of 1,2-fused benzimidazoles and benzo[ <i>d</i> ]imidazoles

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dc.contributor.authorJutamart Saetan
dc.contributor.authorNitchakan Purahong
dc.contributor.authorKannika La‐ongthong
dc.contributor.authorNattawoot Hassa
dc.contributor.authorNawasit Chotsaeng
dc.contributor.authorChutima Kuhakarn
dc.contributor.authorJatuporn Meesin
dc.date.accessioned2026-05-08T19:16:44Z
dc.date.issued2025-1-1
dc.description.abstract-nitroanilines and results in the desired products in yields of up to 99%. A plausible reaction mechanism was proposed on the basis of controlled experiments and cyclic voltammetry (CV) analysis. The benefits of the developed method include one-pot synthesis, open-air conditions, gram-scale synthesis and no requirement for a strong reductant.
dc.identifier.doi10.1039/d5ob00214a
dc.identifier.urihttps://dspace.kmitl.ac.th/handle/123456789/15679
dc.publisherOrganic & Biomolecular Chemistry
dc.subjectNanomaterials for catalytic reactions
dc.subjectElectrocatalysts for Energy Conversion
dc.subjectAmmonia Synthesis and Nitrogen Reduction
dc.titleElectrochemically driven reductive cyclization of <i>o</i> -nitroanilines: synthesis of 1,2-fused benzimidazoles and benzo[ <i>d</i> ]imidazoles
dc.typeArticle

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