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Oxidative Dehydrogenative Couplings of Pyrazol-5-amines Selectively Forming Azopyrroles

[Image: see text] New oxidative dehydrogenative couplings of pyrazol-5-amines for the selective synthesis of azopyrrole derivatives have been described. The former reaction simultaneously installs C–I and N–N bonds through iodination and oxidation, whereas the latter involved a copper-catalyzed oxid...

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Detalles Bibliográficos
Autores principales: Jiang, Bo, Ning, Yi, Fan, Wei, Tu, Shu-Jiang, Li, Guigen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4017612/
https://www.ncbi.nlm.nih.gov/pubmed/24731223
http://dx.doi.org/10.1021/jo5004967
Descripción
Sumario:[Image: see text] New oxidative dehydrogenative couplings of pyrazol-5-amines for the selective synthesis of azopyrrole derivatives have been described. The former reaction simultaneously installs C–I and N–N bonds through iodination and oxidation, whereas the latter involved a copper-catalyzed oxidative coupling process. The resulting iodo-substituted azopyrroles were employed by treatment with various terminal alkynes through Sonogashira cross-coupling leading to new azo compounds.