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Metal–ligand–Lewis acid multi-cooperative catalysis: a step forward in the Conia-ene reaction

An original multi-cooperative catalytic approach was developed by combining metal–ligand cooperation and Lewis acid activation. The [(SCS)Pd](2) complex featuring a non-innocent indenediide-based ligand was found to be a very efficient and versatile catalyst for the Conia-ene reaction, when associat...

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Autores principales: Clerc, Arnaud, Marelli, Enrico, Adet, Nicolas, Monot, Julien, Martín-Vaca, Blanca, Bourissou, Didier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8178805/
https://www.ncbi.nlm.nih.gov/pubmed/34163606
http://dx.doi.org/10.1039/d0sc05036a
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author Clerc, Arnaud
Marelli, Enrico
Adet, Nicolas
Monot, Julien
Martín-Vaca, Blanca
Bourissou, Didier
author_facet Clerc, Arnaud
Marelli, Enrico
Adet, Nicolas
Monot, Julien
Martín-Vaca, Blanca
Bourissou, Didier
author_sort Clerc, Arnaud
collection PubMed
description An original multi-cooperative catalytic approach was developed by combining metal–ligand cooperation and Lewis acid activation. The [(SCS)Pd](2) complex featuring a non-innocent indenediide-based ligand was found to be a very efficient and versatile catalyst for the Conia-ene reaction, when associated with Mg(OTf)(2). The reaction operates at low catalytic loadings under mild conditions with HFIP as a co-solvent. It works with a variety of substrates, including those bearing internal alkynes. It displays complete 5-exo vs. 6-endo regio-selectivity. In addition, except for the highly congested (t)Bu-substituent, the reaction occurs with high Z vs. E stereo-selectivity, making it synthetically useful and complementary to known catalysts.
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spelling pubmed-81788052021-06-22 Metal–ligand–Lewis acid multi-cooperative catalysis: a step forward in the Conia-ene reaction Clerc, Arnaud Marelli, Enrico Adet, Nicolas Monot, Julien Martín-Vaca, Blanca Bourissou, Didier Chem Sci Chemistry An original multi-cooperative catalytic approach was developed by combining metal–ligand cooperation and Lewis acid activation. The [(SCS)Pd](2) complex featuring a non-innocent indenediide-based ligand was found to be a very efficient and versatile catalyst for the Conia-ene reaction, when associated with Mg(OTf)(2). The reaction operates at low catalytic loadings under mild conditions with HFIP as a co-solvent. It works with a variety of substrates, including those bearing internal alkynes. It displays complete 5-exo vs. 6-endo regio-selectivity. In addition, except for the highly congested (t)Bu-substituent, the reaction occurs with high Z vs. E stereo-selectivity, making it synthetically useful and complementary to known catalysts. The Royal Society of Chemistry 2020-10-30 /pmc/articles/PMC8178805/ /pubmed/34163606 http://dx.doi.org/10.1039/d0sc05036a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Clerc, Arnaud
Marelli, Enrico
Adet, Nicolas
Monot, Julien
Martín-Vaca, Blanca
Bourissou, Didier
Metal–ligand–Lewis acid multi-cooperative catalysis: a step forward in the Conia-ene reaction
title Metal–ligand–Lewis acid multi-cooperative catalysis: a step forward in the Conia-ene reaction
title_full Metal–ligand–Lewis acid multi-cooperative catalysis: a step forward in the Conia-ene reaction
title_fullStr Metal–ligand–Lewis acid multi-cooperative catalysis: a step forward in the Conia-ene reaction
title_full_unstemmed Metal–ligand–Lewis acid multi-cooperative catalysis: a step forward in the Conia-ene reaction
title_short Metal–ligand–Lewis acid multi-cooperative catalysis: a step forward in the Conia-ene reaction
title_sort metal–ligand–lewis acid multi-cooperative catalysis: a step forward in the conia-ene reaction
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8178805/
https://www.ncbi.nlm.nih.gov/pubmed/34163606
http://dx.doi.org/10.1039/d0sc05036a
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