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Weinreb Amides as Directing Groups for Transition Metal-Catalyzed C-H Functionalizations
Weinreb amides are a privileged, multi-functional group with well-established utility in classical synthesis. Recently, several studies have demonstrated the use of Weinreb amides as interesting substrates in transition metal-catalyzed C-H functionalization reactions. Herein, we review this part of...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6429370/ https://www.ncbi.nlm.nih.gov/pubmed/30813564 http://dx.doi.org/10.3390/molecules24050830 |
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author | Kalepu, Jagadeesh Pilarski, Lukasz T. |
author_facet | Kalepu, Jagadeesh Pilarski, Lukasz T. |
author_sort | Kalepu, Jagadeesh |
collection | PubMed |
description | Weinreb amides are a privileged, multi-functional group with well-established utility in classical synthesis. Recently, several studies have demonstrated the use of Weinreb amides as interesting substrates in transition metal-catalyzed C-H functionalization reactions. Herein, we review this part of the literature, including the metal catalysts, transformations explored so far and specific insights from mechanistic studies. |
format | Online Article Text |
id | pubmed-6429370 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-64293702019-04-15 Weinreb Amides as Directing Groups for Transition Metal-Catalyzed C-H Functionalizations Kalepu, Jagadeesh Pilarski, Lukasz T. Molecules Review Weinreb amides are a privileged, multi-functional group with well-established utility in classical synthesis. Recently, several studies have demonstrated the use of Weinreb amides as interesting substrates in transition metal-catalyzed C-H functionalization reactions. Herein, we review this part of the literature, including the metal catalysts, transformations explored so far and specific insights from mechanistic studies. MDPI 2019-02-26 /pmc/articles/PMC6429370/ /pubmed/30813564 http://dx.doi.org/10.3390/molecules24050830 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Kalepu, Jagadeesh Pilarski, Lukasz T. Weinreb Amides as Directing Groups for Transition Metal-Catalyzed C-H Functionalizations |
title | Weinreb Amides as Directing Groups for Transition Metal-Catalyzed C-H Functionalizations |
title_full | Weinreb Amides as Directing Groups for Transition Metal-Catalyzed C-H Functionalizations |
title_fullStr | Weinreb Amides as Directing Groups for Transition Metal-Catalyzed C-H Functionalizations |
title_full_unstemmed | Weinreb Amides as Directing Groups for Transition Metal-Catalyzed C-H Functionalizations |
title_short | Weinreb Amides as Directing Groups for Transition Metal-Catalyzed C-H Functionalizations |
title_sort | weinreb amides as directing groups for transition metal-catalyzed c-h functionalizations |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6429370/ https://www.ncbi.nlm.nih.gov/pubmed/30813564 http://dx.doi.org/10.3390/molecules24050830 |
work_keys_str_mv | AT kalepujagadeesh weinrebamidesasdirectinggroupsfortransitionmetalcatalyzedchfunctionalizations AT pilarskilukaszt weinrebamidesasdirectinggroupsfortransitionmetalcatalyzedchfunctionalizations |