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The development of efficient and sustainable methodologies for the synthesis of N -heterocycles is a constant focus of organic synthesis. Herein we report an electrochemical method for the synthesis of… Click to show full abstract
The development of efficient and sustainable methodologies for the synthesis of N -heterocycles is a constant focus of organic synthesis. Herein we report an electrochemical method for the synthesis of benzimidazoles through dehydrogenative cyclization of easily available N-aryl amidines. The reactions are conducted under simple constant current conditions in a undivided cell without need for catalysts, chemical oxidants, or additives and produces H 2 as the only theoretical byproduct.
Keywords:
benzimidazoles via;
synthesis benzimidazoles;
synthesis;
dehydrogenative cyclization;
electrochemical synthesis
Journal Title: ChemSusChem
Year Published: 2021
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Journal Title: ChemSusChem
Year Published: 2021
Link to full text (if available)
Share on Social Media: Sign Up to like & get
recommendations!