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S,O-Ligand-Promoted Palladium-Catalyzed C–H Functionalization Reactions of Nondirected Arenes
[Image: see text] Pd(II)-catalyzed C–H functionalization of nondirected arenes has been realized using an inexpensive and easily accessible type of bidentate S,O-ligand. The catalytic system shows high efficiency in the C–H olefination reaction of electron-rich and electron-poor arenes. This methodo...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5617328/ https://www.ncbi.nlm.nih.gov/pubmed/28966841 http://dx.doi.org/10.1021/acscatal.7b02356 |
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author | Naksomboon, Kananat Valderas, Carolina Gómez-Martínez, Melania Álvarez-Casao, Yolanda Fernández-Ibáñez, M. Ángeles |
author_facet | Naksomboon, Kananat Valderas, Carolina Gómez-Martínez, Melania Álvarez-Casao, Yolanda Fernández-Ibáñez, M. Ángeles |
author_sort | Naksomboon, Kananat |
collection | PubMed |
description | [Image: see text] Pd(II)-catalyzed C–H functionalization of nondirected arenes has been realized using an inexpensive and easily accessible type of bidentate S,O-ligand. The catalytic system shows high efficiency in the C–H olefination reaction of electron-rich and electron-poor arenes. This methodology is operationally simple, scalable, and can be used in late-stage functionalization of complex molecules. The broad applicability of this catalyst has been showcased in other transformations such as Pd(II)-catalyzed C–H acetoxylation and allylation reactions. |
format | Online Article Text |
id | pubmed-5617328 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-56173282017-09-28 S,O-Ligand-Promoted Palladium-Catalyzed C–H Functionalization Reactions of Nondirected Arenes Naksomboon, Kananat Valderas, Carolina Gómez-Martínez, Melania Álvarez-Casao, Yolanda Fernández-Ibáñez, M. Ángeles ACS Catal [Image: see text] Pd(II)-catalyzed C–H functionalization of nondirected arenes has been realized using an inexpensive and easily accessible type of bidentate S,O-ligand. The catalytic system shows high efficiency in the C–H olefination reaction of electron-rich and electron-poor arenes. This methodology is operationally simple, scalable, and can be used in late-stage functionalization of complex molecules. The broad applicability of this catalyst has been showcased in other transformations such as Pd(II)-catalyzed C–H acetoxylation and allylation reactions. American Chemical Society 2017-08-18 2017-09-01 /pmc/articles/PMC5617328/ /pubmed/28966841 http://dx.doi.org/10.1021/acscatal.7b02356 Text en Copyright © 2017 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes. |
spellingShingle | Naksomboon, Kananat Valderas, Carolina Gómez-Martínez, Melania Álvarez-Casao, Yolanda Fernández-Ibáñez, M. Ángeles S,O-Ligand-Promoted Palladium-Catalyzed C–H Functionalization Reactions of Nondirected Arenes |
title | S,O-Ligand-Promoted Palladium-Catalyzed C–H
Functionalization Reactions of Nondirected Arenes |
title_full | S,O-Ligand-Promoted Palladium-Catalyzed C–H
Functionalization Reactions of Nondirected Arenes |
title_fullStr | S,O-Ligand-Promoted Palladium-Catalyzed C–H
Functionalization Reactions of Nondirected Arenes |
title_full_unstemmed | S,O-Ligand-Promoted Palladium-Catalyzed C–H
Functionalization Reactions of Nondirected Arenes |
title_short | S,O-Ligand-Promoted Palladium-Catalyzed C–H
Functionalization Reactions of Nondirected Arenes |
title_sort | s,o-ligand-promoted palladium-catalyzed c–h
functionalization reactions of nondirected arenes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5617328/ https://www.ncbi.nlm.nih.gov/pubmed/28966841 http://dx.doi.org/10.1021/acscatal.7b02356 |
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