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Revisiting the Chemistry of Vinylpyrazoles: Properties, Synthesis, and Reactivity

Vinylpyrazoles, also known as pyrazolyl olefins, are interesting motifs in organic chemistry but have been overlooked. This review describes the properties and synthetic routes of vinylpyrazoles and highlights their versatility as building blocks for the construction of more complex organic molecule...

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Autores principales: Silva, Vera L. M., Silva, Artur M. S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9182008/
https://www.ncbi.nlm.nih.gov/pubmed/35684432
http://dx.doi.org/10.3390/molecules27113493
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author Silva, Vera L. M.
Silva, Artur M. S.
author_facet Silva, Vera L. M.
Silva, Artur M. S.
author_sort Silva, Vera L. M.
collection PubMed
description Vinylpyrazoles, also known as pyrazolyl olefins, are interesting motifs in organic chemistry but have been overlooked. This review describes the properties and synthetic routes of vinylpyrazoles and highlights their versatility as building blocks for the construction of more complex organic molecules. Concerning the reactivity of vinylpyrazoles, the topics surveyed herein include their use in cycloaddition reactions, free-radical polymerizations, halogenation and hydrohalogenation reactions, and more recently in transition-metal-catalyzed reactions, among other transformations. The current state of the art about vinylpyrazoles is presented with an eye to future developments regarding the chemistry of these interesting compounds. Styrylpyrazoles were not considered in this review, as they were the subject of a previous review article published in 2020.
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spelling pubmed-91820082022-06-10 Revisiting the Chemistry of Vinylpyrazoles: Properties, Synthesis, and Reactivity Silva, Vera L. M. Silva, Artur M. S. Molecules Review Vinylpyrazoles, also known as pyrazolyl olefins, are interesting motifs in organic chemistry but have been overlooked. This review describes the properties and synthetic routes of vinylpyrazoles and highlights their versatility as building blocks for the construction of more complex organic molecules. Concerning the reactivity of vinylpyrazoles, the topics surveyed herein include their use in cycloaddition reactions, free-radical polymerizations, halogenation and hydrohalogenation reactions, and more recently in transition-metal-catalyzed reactions, among other transformations. The current state of the art about vinylpyrazoles is presented with an eye to future developments regarding the chemistry of these interesting compounds. Styrylpyrazoles were not considered in this review, as they were the subject of a previous review article published in 2020. MDPI 2022-05-29 /pmc/articles/PMC9182008/ /pubmed/35684432 http://dx.doi.org/10.3390/molecules27113493 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Silva, Vera L. M.
Silva, Artur M. S.
Revisiting the Chemistry of Vinylpyrazoles: Properties, Synthesis, and Reactivity
title Revisiting the Chemistry of Vinylpyrazoles: Properties, Synthesis, and Reactivity
title_full Revisiting the Chemistry of Vinylpyrazoles: Properties, Synthesis, and Reactivity
title_fullStr Revisiting the Chemistry of Vinylpyrazoles: Properties, Synthesis, and Reactivity
title_full_unstemmed Revisiting the Chemistry of Vinylpyrazoles: Properties, Synthesis, and Reactivity
title_short Revisiting the Chemistry of Vinylpyrazoles: Properties, Synthesis, and Reactivity
title_sort revisiting the chemistry of vinylpyrazoles: properties, synthesis, and reactivity
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9182008/
https://www.ncbi.nlm.nih.gov/pubmed/35684432
http://dx.doi.org/10.3390/molecules27113493
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