ArticleOrganic letters2013
Facile Cu(I)-catalyzed oxidative coupling of anilines to azo compounds and hydrazines with diaziridinone under mild conditions.
Article in Organic letters, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.
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Who cites it
15 citing papers in PubMed.
- Article
- Protocol for microwave-assisted synthesis of unsymmetrical azo dyes.STAR protocols · 2022Article
- Organocatalytic Reduction of Aromatic Nitro Compounds: The Use of Solid-Supported Phenyl(2-quinolyl)methanol.ACS omega · 2022Article
- Microwave-assisted rapid and sustainable synthesis of unsymmetrical azo dyes by coupling of nitroarenes with aniline derivatives.iScience · 2022Article
- Synthesis and photochromism of catechol-containing symmetrical azobenzene compounds.Royal Society open science · 2022Article
- Novel and Sustainable Colorants Developed via Incorporating Azo Chromophores into Dopamine Molecules.ACS omega · 2022Article
- Cross-dehydrogenative N-N couplings.Chemical science · 2021Review
- Azo synthesis meets molecular iodine catalysis.RSC advances · 2021Article
- Article
- Article
- Visible Light-Emitting Diode Light-Driven CuACS omega · 2019Article
- Cu-Catalyzed Aerobic Oxidative N-N Coupling of Carbazoles and Diarylamines Including Selective Cross-Coupling.Journal of the American Chemical Society · 2018Article
- Synthesis of mono-functionalized S-diazocines via intramolecular Baeyer-Mills reactions.Beilstein journal of organic chemistry · 2018Article
- Copper-catalyzed oxidative homo- and cross-coupling of Grignard reagents using diaziridinone.Organic letters · 2014Article
- A facile copper(I)-catalyzed homocoupling of terminal alkynes to 1,3-diynes with diaziridinone under mild conditions.Organic & biomolecular chemistry · 2013Article
Corrections and comments
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Authors and funding
2 authors.
Funding
Abstract
A mild and highly efficient Cu(I)-catalyzed oxidative coupling of anilines is described. Various primary and secondary anilines can be efficiently coupled under mild conditions to the corresponding azo compounds and hydrazines in high yields. This method provides a direct and practical access to these compounds and is also amenable to gram scale with no special precautions to exclude air or moisture.
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