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Denitrative Cross-Couplings of Nitrostyrenes
Interestingly, β-nitrostyrenes, typically bench stable compounds, are highly promising cross-coupling partners, due to their excellent availability and well understood reactivity. In this review, we report on the discovery and advancements, in the field of stereoselective, denitrative cross-coupling...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7435674/ https://www.ncbi.nlm.nih.gov/pubmed/32726964 http://dx.doi.org/10.3390/molecules25153390 |
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author | Marčeková, Michaela Ferko, Branislav Detková, Katarína Ráchel Jakubec, Pavol |
author_facet | Marčeková, Michaela Ferko, Branislav Detková, Katarína Ráchel Jakubec, Pavol |
author_sort | Marčeková, Michaela |
collection | PubMed |
description | Interestingly, β-nitrostyrenes, typically bench stable compounds, are highly promising cross-coupling partners, due to their excellent availability and well understood reactivity. In this review, we report on the discovery and advancements, in the field of stereoselective, denitrative cross-couplings of β-nitrostyrenes with miscellaneous organic reagents. The rapidly expanding field offers alternative access to a broad range of functionalized alkenes, including β-alkylated styrenes, chalcones, stilbenes, cinnamic acids, and conjugated sulfones and phosphonates. The most important mechanistic pathways are briefly discussed, to familiarize readers with the elementary reactions occurring during the coupling. |
format | Online Article Text |
id | pubmed-7435674 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-74356742020-08-28 Denitrative Cross-Couplings of Nitrostyrenes Marčeková, Michaela Ferko, Branislav Detková, Katarína Ráchel Jakubec, Pavol Molecules Review Interestingly, β-nitrostyrenes, typically bench stable compounds, are highly promising cross-coupling partners, due to their excellent availability and well understood reactivity. In this review, we report on the discovery and advancements, in the field of stereoselective, denitrative cross-couplings of β-nitrostyrenes with miscellaneous organic reagents. The rapidly expanding field offers alternative access to a broad range of functionalized alkenes, including β-alkylated styrenes, chalcones, stilbenes, cinnamic acids, and conjugated sulfones and phosphonates. The most important mechanistic pathways are briefly discussed, to familiarize readers with the elementary reactions occurring during the coupling. MDPI 2020-07-27 /pmc/articles/PMC7435674/ /pubmed/32726964 http://dx.doi.org/10.3390/molecules25153390 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Marčeková, Michaela Ferko, Branislav Detková, Katarína Ráchel Jakubec, Pavol Denitrative Cross-Couplings of Nitrostyrenes |
title | Denitrative Cross-Couplings of Nitrostyrenes |
title_full | Denitrative Cross-Couplings of Nitrostyrenes |
title_fullStr | Denitrative Cross-Couplings of Nitrostyrenes |
title_full_unstemmed | Denitrative Cross-Couplings of Nitrostyrenes |
title_short | Denitrative Cross-Couplings of Nitrostyrenes |
title_sort | denitrative cross-couplings of nitrostyrenes |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7435674/ https://www.ncbi.nlm.nih.gov/pubmed/32726964 http://dx.doi.org/10.3390/molecules25153390 |
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