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Palladium and Organocatalysis: An Excellent Recipe for Asymmetric Synthesis
The dual activation of simple substrates by the combination of organocatalysis and palladium catalysis has been successfully applied in a variety of different asymmetric transformations. Thus, the asymmetric α-allylation of carbonyl compounds, α-fluorination of acyl derivatives, decarboxylative prot...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270479/ https://www.ncbi.nlm.nih.gov/pubmed/23973988 http://dx.doi.org/10.3390/molecules180910108 |
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author | Fernández-Ibañez, M. Ángeles Maciá, Beatriz Alonso, Diego A. Pastor, Isidro M. |
author_facet | Fernández-Ibañez, M. Ángeles Maciá, Beatriz Alonso, Diego A. Pastor, Isidro M. |
author_sort | Fernández-Ibañez, M. Ángeles |
collection | PubMed |
description | The dual activation of simple substrates by the combination of organocatalysis and palladium catalysis has been successfully applied in a variety of different asymmetric transformations. Thus, the asymmetric α-allylation of carbonyl compounds, α-fluorination of acyl derivatives, decarboxylative protonation of β-dicarbonyl compounds, cyclization reactions of alkynyl carbonyl compounds and β-functionalization of aldehydes have been efficiently achieved employing this double-catalytic methodology. |
format | Online Article Text |
id | pubmed-6270479 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62704792018-12-18 Palladium and Organocatalysis: An Excellent Recipe for Asymmetric Synthesis Fernández-Ibañez, M. Ángeles Maciá, Beatriz Alonso, Diego A. Pastor, Isidro M. Molecules Review The dual activation of simple substrates by the combination of organocatalysis and palladium catalysis has been successfully applied in a variety of different asymmetric transformations. Thus, the asymmetric α-allylation of carbonyl compounds, α-fluorination of acyl derivatives, decarboxylative protonation of β-dicarbonyl compounds, cyclization reactions of alkynyl carbonyl compounds and β-functionalization of aldehydes have been efficiently achieved employing this double-catalytic methodology. MDPI 2013-08-22 /pmc/articles/PMC6270479/ /pubmed/23973988 http://dx.doi.org/10.3390/molecules180910108 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Review Fernández-Ibañez, M. Ángeles Maciá, Beatriz Alonso, Diego A. Pastor, Isidro M. Palladium and Organocatalysis: An Excellent Recipe for Asymmetric Synthesis |
title | Palladium and Organocatalysis: An Excellent Recipe for Asymmetric Synthesis |
title_full | Palladium and Organocatalysis: An Excellent Recipe for Asymmetric Synthesis |
title_fullStr | Palladium and Organocatalysis: An Excellent Recipe for Asymmetric Synthesis |
title_full_unstemmed | Palladium and Organocatalysis: An Excellent Recipe for Asymmetric Synthesis |
title_short | Palladium and Organocatalysis: An Excellent Recipe for Asymmetric Synthesis |
title_sort | palladium and organocatalysis: an excellent recipe for asymmetric synthesis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270479/ https://www.ncbi.nlm.nih.gov/pubmed/23973988 http://dx.doi.org/10.3390/molecules180910108 |
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