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Iron-Catalyzed Acceptorless Dehydrogenative Coupling of Alcohols With Aromatic Diamines: Selective Synthesis of 1,2-Disubstituted Benzimidazoles
Benzimidazoles are important -heteroaromatic compounds with various biological activities and pharmacological applications. Herein, we present the first iron-catalyzed selective synthesis of 1,2-disubstituted benzimidazoles acceptorless dehydrogenative coupling of primary alcohols with aromatic diam...
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Published in: | Frontiers in chemistry 2020-06, Vol.8, p.429-429 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Benzimidazoles are important
-heteroaromatic compounds with various biological activities and pharmacological applications. Herein, we present the first iron-catalyzed selective synthesis of 1,2-disubstituted benzimidazoles
acceptorless dehydrogenative coupling of primary alcohols with aromatic diamines. The tricarbonyl (η
-cyclopentadienone) iron complex catalyzed dehydrogenative cyclization, releasing water and hydrogen gas as by-products. The earth abundance and low toxicity of iron metal enable the provision of an eco-friendly and efficient catalytic method for the synthesis of benzimidazoles. |
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ISSN: | 2296-2646 2296-2646 |
DOI: | 10.3389/fchem.2020.00429 |