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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2014
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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. |
format | Online Article Text |
id | pubmed-4017612 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
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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