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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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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. |
format | Online Article Text |
id | pubmed-9299716 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT kreuzahlermathis metalcatalyzedhaloalkynylationreactions AT haberhauergebhard metalcatalyzedhaloalkynylationreactions |