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...

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Published in:Molecules
Main Authors: Fernández-Ibañez, M. Ángeles, Maciá, Beatriz, Alonso, Diego A., Pastor, Isidro M.
Other Authors: UAM. Departamento de Química Orgánica
Format: Article in Journal/Newspaper
Language:English
Published: MDPI 2015
Subjects:
Online Access:http://hdl.handle.net/10486/667528
https://doi.org/10.3390/molecules180910108
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spelling ftuamadrid:oai:repositorio.uam.es:10486/667528 2023-05-15T17:53:47+02:00 Palladium and organocatalysis: An excellent recipe for asymmetric synthesis Fernández-Ibañez, M. Ángeles Maciá, Beatriz Alonso, Diego A. Pastor, Isidro M. UAM. Departamento de Química Orgánica 2015-07-23T08:02:24Z application/pdf http://hdl.handle.net/10486/667528 https://doi.org/10.3390/molecules180910108 eng eng MDPI Molecules http://dx.doi.org/10.3390/molecules180910108 Comunidad de Madrid. S2009/PPQ-1634/AVANCAT Molecules 18.9 (2013): 10108-10121 1420-3049 http://hdl.handle.net/10486/667528 doi:10.3390/molecules180910108 10108 9 10121 18 © 2013 by the authors Reconocimiento openAccess Allylation Asymmetric synthesis Decarboxylative protonation Dual activation Fluorination Organocatalysis Palladium Tandem reaction Química article info:eu-repo/semantics/publishedVersion 2015 ftuamadrid https://doi.org/10.3390/molecules180910108 2022-05-10T23:16:35Z 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 MAFI thanks financial support from the Ministerio de Economía y Competitividad MINECO, CTQ 2012-35790) and the Consejería de Educación de la Comunidad de Madrid (AVANCAT, S2009/PPQ-1634). BM thanks the European Commission for a Marie Curie Integration Grant (FP7-PEOPLE-2012-CIG). IMP thanks financial support from the Ministerio de Ciencia e Innovación (MICINN) of Spain (CTQ2011-24165) and from the University of Alicante. DAA thanks financial support for the European Union (ORCA action CM0905) and from the University of Alicante Article in Journal/Newspaper Orca Universidad Autónoma de Madrid (UAM): Biblos-e Archivo Molecules 18 9 10108 10121
institution Open Polar
collection Universidad Autónoma de Madrid (UAM): Biblos-e Archivo
op_collection_id ftuamadrid
language English
topic Allylation
Asymmetric synthesis
Decarboxylative protonation
Dual activation
Fluorination
Organocatalysis
Palladium
Tandem reaction
Química
spellingShingle Allylation
Asymmetric synthesis
Decarboxylative protonation
Dual activation
Fluorination
Organocatalysis
Palladium
Tandem reaction
Química
Fernández-Ibañez, M. Ángeles
Maciá, Beatriz
Alonso, Diego A.
Pastor, Isidro M.
Palladium and organocatalysis: An excellent recipe for asymmetric synthesis
topic_facet Allylation
Asymmetric synthesis
Decarboxylative protonation
Dual activation
Fluorination
Organocatalysis
Palladium
Tandem reaction
Química
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 MAFI thanks financial support from the Ministerio de Economía y Competitividad MINECO, CTQ 2012-35790) and the Consejería de Educación de la Comunidad de Madrid (AVANCAT, S2009/PPQ-1634). BM thanks the European Commission for a Marie Curie Integration Grant (FP7-PEOPLE-2012-CIG). IMP thanks financial support from the Ministerio de Ciencia e Innovación (MICINN) of Spain (CTQ2011-24165) and from the University of Alicante. DAA thanks financial support for the European Union (ORCA action CM0905) and from the University of Alicante
author2 UAM. Departamento de Química Orgánica
format Article in Journal/Newspaper
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
title Palladium and organocatalysis: An excellent recipe for asymmetric synthesis
title_short 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_sort palladium and organocatalysis: an excellent recipe for asymmetric synthesis
publisher MDPI
publishDate 2015
url http://hdl.handle.net/10486/667528
https://doi.org/10.3390/molecules180910108
genre Orca
genre_facet Orca
op_relation Molecules
http://dx.doi.org/10.3390/molecules180910108
Comunidad de Madrid. S2009/PPQ-1634/AVANCAT
Molecules 18.9 (2013): 10108-10121
1420-3049
http://hdl.handle.net/10486/667528
doi:10.3390/molecules180910108
10108
9
10121
18
op_rights © 2013 by the authors
Reconocimiento
openAccess
op_doi https://doi.org/10.3390/molecules180910108
container_title Molecules
container_volume 18
container_issue 9
container_start_page 10108
op_container_end_page 10121
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