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Photoredox Catalysis in Organic Chemistry

[Image: see text] In recent years, photoredox catalysis has come to the forefront in organic chemistry as a powerful strategy for the activation of small molecules. In a general sense, these approaches rely on the ability of metal complexes and organic dyes to convert visible light into chemical ene...

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Autores principales: Shaw, Megan H., Twilton, Jack, MacMillan, David W. C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2016
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4994065/
https://www.ncbi.nlm.nih.gov/pubmed/27477076
http://dx.doi.org/10.1021/acs.joc.6b01449
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author Shaw, Megan H.
Twilton, Jack
MacMillan, David W. C.
author_facet Shaw, Megan H.
Twilton, Jack
MacMillan, David W. C.
author_sort Shaw, Megan H.
collection PubMed
description [Image: see text] In recent years, photoredox catalysis has come to the forefront in organic chemistry as a powerful strategy for the activation of small molecules. In a general sense, these approaches rely on the ability of metal complexes and organic dyes to convert visible light into chemical energy by engaging in single-electron transfer with organic substrates, thereby generating reactive intermediates. In this Perspective, we highlight the unique ability of photoredox catalysis to expedite the development of completely new reaction mechanisms, with particular emphasis placed on multicatalytic strategies that enable the construction of challenging carbon–carbon and carbon–heteroatom bonds.
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spelling pubmed-49940652016-08-24 Photoredox Catalysis in Organic Chemistry Shaw, Megan H. Twilton, Jack MacMillan, David W. C. J Org Chem [Image: see text] In recent years, photoredox catalysis has come to the forefront in organic chemistry as a powerful strategy for the activation of small molecules. In a general sense, these approaches rely on the ability of metal complexes and organic dyes to convert visible light into chemical energy by engaging in single-electron transfer with organic substrates, thereby generating reactive intermediates. In this Perspective, we highlight the unique ability of photoredox catalysis to expedite the development of completely new reaction mechanisms, with particular emphasis placed on multicatalytic strategies that enable the construction of challenging carbon–carbon and carbon–heteroatom bonds. American Chemical Society 2016-08-01 2016-08-19 /pmc/articles/PMC4994065/ /pubmed/27477076 http://dx.doi.org/10.1021/acs.joc.6b01449 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 Shaw, Megan H.
Twilton, Jack
MacMillan, David W. C.
Photoredox Catalysis in Organic Chemistry
title Photoredox Catalysis in Organic Chemistry
title_full Photoredox Catalysis in Organic Chemistry
title_fullStr Photoredox Catalysis in Organic Chemistry
title_full_unstemmed Photoredox Catalysis in Organic Chemistry
title_short Photoredox Catalysis in Organic Chemistry
title_sort photoredox catalysis in organic chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4994065/
https://www.ncbi.nlm.nih.gov/pubmed/27477076
http://dx.doi.org/10.1021/acs.joc.6b01449
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