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Homogeneous Manganese-Catalyzed Hydrofunctionalizations of Alkenes and Alkynes: Catalytic and Mechanistic Tendencies
[Image: see text] In recent years, many manganese-based homogeneous catalytic precursors have been developed as powerful alternatives in organic synthesis. Among these, the hydrofunctionalizations of unsaturated C–C bonds correspond to outstanding ways to afford compounds with more versatile functio...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9608411/ https://www.ncbi.nlm.nih.gov/pubmed/36312376 http://dx.doi.org/10.1021/acsomega.2c05109 |
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author | Torres-Calis, Antonio García, Juventino J. |
author_facet | Torres-Calis, Antonio García, Juventino J. |
author_sort | Torres-Calis, Antonio |
collection | PubMed |
description | [Image: see text] In recent years, many manganese-based homogeneous catalytic precursors have been developed as powerful alternatives in organic synthesis. Among these, the hydrofunctionalizations of unsaturated C–C bonds correspond to outstanding ways to afford compounds with more versatile functional groups, which are commonly used as building blocks in the production of fine chemicals and feedstock for the industrial field. Herein, we present an account of the Mn-catalyzed homogeneous hydrofunctionalizations of alkenes and alkynes with the main objective of finding catalytic and mechanistic tendencies that could serve as a platform for the works to come. |
format | Online Article Text |
id | pubmed-9608411 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-96084112022-10-28 Homogeneous Manganese-Catalyzed Hydrofunctionalizations of Alkenes and Alkynes: Catalytic and Mechanistic Tendencies Torres-Calis, Antonio García, Juventino J. ACS Omega [Image: see text] In recent years, many manganese-based homogeneous catalytic precursors have been developed as powerful alternatives in organic synthesis. Among these, the hydrofunctionalizations of unsaturated C–C bonds correspond to outstanding ways to afford compounds with more versatile functional groups, which are commonly used as building blocks in the production of fine chemicals and feedstock for the industrial field. Herein, we present an account of the Mn-catalyzed homogeneous hydrofunctionalizations of alkenes and alkynes with the main objective of finding catalytic and mechanistic tendencies that could serve as a platform for the works to come. American Chemical Society 2022-10-11 /pmc/articles/PMC9608411/ /pubmed/36312376 http://dx.doi.org/10.1021/acsomega.2c05109 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Torres-Calis, Antonio García, Juventino J. Homogeneous Manganese-Catalyzed Hydrofunctionalizations of Alkenes and Alkynes: Catalytic and Mechanistic Tendencies |
title | Homogeneous Manganese-Catalyzed Hydrofunctionalizations
of Alkenes and Alkynes: Catalytic and Mechanistic Tendencies |
title_full | Homogeneous Manganese-Catalyzed Hydrofunctionalizations
of Alkenes and Alkynes: Catalytic and Mechanistic Tendencies |
title_fullStr | Homogeneous Manganese-Catalyzed Hydrofunctionalizations
of Alkenes and Alkynes: Catalytic and Mechanistic Tendencies |
title_full_unstemmed | Homogeneous Manganese-Catalyzed Hydrofunctionalizations
of Alkenes and Alkynes: Catalytic and Mechanistic Tendencies |
title_short | Homogeneous Manganese-Catalyzed Hydrofunctionalizations
of Alkenes and Alkynes: Catalytic and Mechanistic Tendencies |
title_sort | homogeneous manganese-catalyzed hydrofunctionalizations
of alkenes and alkynes: catalytic and mechanistic tendencies |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9608411/ https://www.ncbi.nlm.nih.gov/pubmed/36312376 http://dx.doi.org/10.1021/acsomega.2c05109 |
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