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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...

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Autores principales: Marčeková, Michaela, Ferko, Branislav, Detková, Katarína Ráchel, Jakubec, Pavol
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
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.
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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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