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Metal‐Catalyzed Haloalkynylation Reactions

Metal catalysis has revolutionized synthetic chemistry, leading to entirely new, very efficient transformations, which enable access to complex functionalized molecules. One such new transformation method is the haloalkynylation reaction, in which both a halogen atom and an alkynyl unit are transfer...

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Detalles Bibliográficos
Autores principales: Kreuzahler, Mathis, Haberhauer, Gebhard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9299716/
https://www.ncbi.nlm.nih.gov/pubmed/34644433
http://dx.doi.org/10.1002/chem.202103046
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author Kreuzahler, Mathis
Haberhauer, Gebhard
author_facet Kreuzahler, Mathis
Haberhauer, Gebhard
author_sort Kreuzahler, Mathis
collection PubMed
description Metal catalysis has revolutionized synthetic chemistry, leading to entirely new, very efficient transformations, which enable access to complex functionalized molecules. One such new transformation method is the haloalkynylation reaction, in which both a halogen atom and an alkynyl unit are transferred to an unsaturated carbon‐carbon bond. This minireview summarizes the development of metal‐catalyzed haloalkynylation reactions since their beginning about a decade ago. So far, arynes, alkenes and alkynes have been used as unsaturated systems and the reactivities of these systems are summarized in individual chapters of the minireview. Especially, the last few years have witnessed a rapid development due to gold‐catalyzed reactions. Here, we discuss how the choice of the catalytic system influences the regio‐ and stereoselectivity of the addition.
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spelling pubmed-92997162022-07-21 Metal‐Catalyzed Haloalkynylation Reactions Kreuzahler, Mathis Haberhauer, Gebhard Chemistry Minireviews Metal catalysis has revolutionized synthetic chemistry, leading to entirely new, very efficient transformations, which enable access to complex functionalized molecules. One such new transformation method is the haloalkynylation reaction, in which both a halogen atom and an alkynyl unit are transferred to an unsaturated carbon‐carbon bond. This minireview summarizes the development of metal‐catalyzed haloalkynylation reactions since their beginning about a decade ago. So far, arynes, alkenes and alkynes have been used as unsaturated systems and the reactivities of these systems are summarized in individual chapters of the minireview. Especially, the last few years have witnessed a rapid development due to gold‐catalyzed reactions. Here, we discuss how the choice of the catalytic system influences the regio‐ and stereoselectivity of the addition. John Wiley and Sons Inc. 2021-11-18 2022-01-19 /pmc/articles/PMC9299716/ /pubmed/34644433 http://dx.doi.org/10.1002/chem.202103046 Text en © 2021 The Authors. Chemistry - A European Journal published by Wiley-VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Minireviews
Kreuzahler, Mathis
Haberhauer, Gebhard
Metal‐Catalyzed Haloalkynylation Reactions
title Metal‐Catalyzed Haloalkynylation Reactions
title_full Metal‐Catalyzed Haloalkynylation Reactions
title_fullStr Metal‐Catalyzed Haloalkynylation Reactions
title_full_unstemmed Metal‐Catalyzed Haloalkynylation Reactions
title_short Metal‐Catalyzed Haloalkynylation Reactions
title_sort metal‐catalyzed haloalkynylation reactions
topic Minireviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9299716/
https://www.ncbi.nlm.nih.gov/pubmed/34644433
http://dx.doi.org/10.1002/chem.202103046
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