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Green Approach for the Domino Reduction/Reductive Amination of Nitroarenes and Chemoselective Reduction of Aldehydes Using Fe/aq.Citric Acid/Montmorillonite K10

机译:使用Fe/aq.citric Acid/Montmorillonite K10的硝化胺和化学选择性还原的绿色方法降低/还原性胺化和化学选择性还原

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摘要

We have developed a new and mild method for the direct onepot reduction/reductive amination of nitroarenes with arylaldehydes using Fe/aq citric acid/montmorillonite K10 catalytic system under ambient conditions.This catalyst has excellent functional group compatibility and the reaction provides rapid access to a diverse range of secondary amines.Under the conditions,aromatic aldehydes are selectively reduced to benzyl alcohols in the presence of ketones.A concise and efficient approach to the synthesis of diverse range of 1,2-disubstituted benzimidazoles has also been accomplished for the first time from 1,2-dinitrobenzene and aromatic aldehydes using the above catalytic system.The method involves the domino nitro reduction/cyclization/reduction cascade.
机译:我们已经开发了一种新的温和方法,用于使用Fe/aq柠檬酸/蒙特米龙甲酸/montmorillonite k10催化系统在环境条件下直接减少/还原硝基苯甲酸的胺化/还原性胺化。 在条件下,在存在酮的情况下,芳香醛在条件下选择性降低为苄醇。一种简洁有效的方法,即首次完成1,2二取代的苯咪唑多种范围的合成方法。 使用上述催化系统从1,2-二硝基苯和芳香醛。该方法涉及多米诺硝基减少/环化/还原级联。

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