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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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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
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author Jiang, Bo
Ning, Yi
Fan, Wei
Tu, Shu-Jiang
Li, Guigen
author_facet Jiang, Bo
Ning, Yi
Fan, Wei
Tu, Shu-Jiang
Li, Guigen
author_sort Jiang, Bo
collection PubMed
description [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.
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spelling pubmed-40176122015-04-14 Oxidative Dehydrogenative Couplings of Pyrazol-5-amines Selectively Forming Azopyrroles Jiang, Bo Ning, Yi Fan, Wei Tu, Shu-Jiang Li, Guigen J Org Chem [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. American Chemical Society 2014-04-14 2014-05-02 /pmc/articles/PMC4017612/ /pubmed/24731223 http://dx.doi.org/10.1021/jo5004967 Text en Copyright © 2014 American Chemical Society
spellingShingle Jiang, Bo
Ning, Yi
Fan, Wei
Tu, Shu-Jiang
Li, Guigen
Oxidative Dehydrogenative Couplings of Pyrazol-5-amines Selectively Forming Azopyrroles
title Oxidative Dehydrogenative Couplings of Pyrazol-5-amines Selectively Forming Azopyrroles
title_full Oxidative Dehydrogenative Couplings of Pyrazol-5-amines Selectively Forming Azopyrroles
title_fullStr Oxidative Dehydrogenative Couplings of Pyrazol-5-amines Selectively Forming Azopyrroles
title_full_unstemmed Oxidative Dehydrogenative Couplings of Pyrazol-5-amines Selectively Forming Azopyrroles
title_short Oxidative Dehydrogenative Couplings of Pyrazol-5-amines Selectively Forming Azopyrroles
title_sort oxidative dehydrogenative couplings of pyrazol-5-amines selectively forming azopyrroles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4017612/
https://www.ncbi.nlm.nih.gov/pubmed/24731223
http://dx.doi.org/10.1021/jo5004967
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