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Photoredox Catalysis Unlocks Single-Electron Elementary Steps in Transition Metal Catalyzed Cross-Coupling
[Image: see text] Since initial reports, cross-coupling technologies employing photoredox catalysts to access novel reactivity have developed with increasing pace. In this Outlook, prominent examples from the recent literature are organized on the basis of the elementary transformation enabled by ph...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4882737/ https://www.ncbi.nlm.nih.gov/pubmed/27280163 http://dx.doi.org/10.1021/acscentsci.6b00090 |
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author | Levin, Mark D. Kim, Suhong Toste, F. Dean |
author_facet | Levin, Mark D. Kim, Suhong Toste, F. Dean |
author_sort | Levin, Mark D. |
collection | PubMed |
description | [Image: see text] Since initial reports, cross-coupling technologies employing photoredox catalysts to access novel reactivity have developed with increasing pace. In this Outlook, prominent examples from the recent literature are organized on the basis of the elementary transformation enabled by photoredox catalysis and are discussed in the context of relevant historical precedent in stoichiometric organometallic chemistry. This treatment allows mechanistic similarities inherent to odd-electron transition metal reactivity to be generalized to a set of lessons for future reaction development. |
format | Online Article Text |
id | pubmed-4882737 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-48827372016-06-08 Photoredox Catalysis Unlocks Single-Electron Elementary Steps in Transition Metal Catalyzed Cross-Coupling Levin, Mark D. Kim, Suhong Toste, F. Dean ACS Cent Sci [Image: see text] Since initial reports, cross-coupling technologies employing photoredox catalysts to access novel reactivity have developed with increasing pace. In this Outlook, prominent examples from the recent literature are organized on the basis of the elementary transformation enabled by photoredox catalysis and are discussed in the context of relevant historical precedent in stoichiometric organometallic chemistry. This treatment allows mechanistic similarities inherent to odd-electron transition metal reactivity to be generalized to a set of lessons for future reaction development. American Chemical Society 2016-05-03 2016-05-25 /pmc/articles/PMC4882737/ /pubmed/27280163 http://dx.doi.org/10.1021/acscentsci.6b00090 Text en Copyright © 2016 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Levin, Mark D. Kim, Suhong Toste, F. Dean Photoredox Catalysis Unlocks Single-Electron Elementary Steps in Transition Metal Catalyzed Cross-Coupling |
title | Photoredox Catalysis Unlocks Single-Electron Elementary
Steps in Transition Metal Catalyzed Cross-Coupling |
title_full | Photoredox Catalysis Unlocks Single-Electron Elementary
Steps in Transition Metal Catalyzed Cross-Coupling |
title_fullStr | Photoredox Catalysis Unlocks Single-Electron Elementary
Steps in Transition Metal Catalyzed Cross-Coupling |
title_full_unstemmed | Photoredox Catalysis Unlocks Single-Electron Elementary
Steps in Transition Metal Catalyzed Cross-Coupling |
title_short | Photoredox Catalysis Unlocks Single-Electron Elementary
Steps in Transition Metal Catalyzed Cross-Coupling |
title_sort | photoredox catalysis unlocks single-electron elementary
steps in transition metal catalyzed cross-coupling |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4882737/ https://www.ncbi.nlm.nih.gov/pubmed/27280163 http://dx.doi.org/10.1021/acscentsci.6b00090 |
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