ArticleThe Journal of organic chemistry2015
Synthesis of 2-Aminoazoles from Thioesters via α-Heterosubstituted Ketones by Copper-Mediated Cross-Coupling.
Article in The Journal of organic chemistry, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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Who cites it
4 citing papers in PubMed, 35 citations in OpenAlex.
- An Enantioselective Decarboxylative Glycolate Aldol Reaction.Organic letters · 2024Article
- Synthetic Efforts toward the Synthesis of a Fluorinated Analog of 5-Aminolevulinic Acid: Practical Synthesis of Racemic and Enantiomerically Defined 3-Fluoro-5-aminolevulinic Acid.The Journal of organic chemistry · 2024Article
- Synthesis of α-heterosubstituted ketones through sulfur mediated difunctionalization of internal alkynes.Chemical science · 2019Article
- An Expeditious and Greener Synthesis of 2-Aminoimidazoles in Deep Eutectic Solvents.Molecules (Basel, Switzerland) · 2016Article
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Authors and funding
3 authors at 1 institution in 2 countries.
Funding
Abstract
Facile synthesis of a variety of α-heterosubstituted ketones under mild conditions was achieved by copper-mediated cross-coupling of thioesters with functionalized organostannanes. Application of this coupling methodology provided a concise pathway for the conversion of carboxylic acids to 2-aminoimidazoles, 2-aminothiazoles, and 2-aminooxazoles via thioesters in practical yields.
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Registered trials
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