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Direct Arylation in the Presence of Palladium Pincer Complexes

Direct arylation is an atom-economical alternative to more established procedures such as Stille, Suzuki or Negishi arylation reactions. In comparison with other palladium sources and ligands, the use of palladium pincer complexes as catalysts or pre-catalysts for direct arylation has resulted in im...

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Autores principales: Urgoitia, Garazi, Herrero, Maria Teresa, Churruca, Fátima, Conde, Nerea, SanMartin, Raul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8305722/
https://www.ncbi.nlm.nih.gov/pubmed/34299661
http://dx.doi.org/10.3390/molecules26144385
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author Urgoitia, Garazi
Herrero, Maria Teresa
Churruca, Fátima
Conde, Nerea
SanMartin, Raul
author_facet Urgoitia, Garazi
Herrero, Maria Teresa
Churruca, Fátima
Conde, Nerea
SanMartin, Raul
author_sort Urgoitia, Garazi
collection PubMed
description Direct arylation is an atom-economical alternative to more established procedures such as Stille, Suzuki or Negishi arylation reactions. In comparison with other palladium sources and ligands, the use of palladium pincer complexes as catalysts or pre-catalysts for direct arylation has resulted in improved efficiency, higher reaction yields, and advantageous reaction conditions. In addition to a revision of the literature concerning intra- and intermolecular direct arylation reactions performed in the presence of palladium pincer complexes, the role of these remarkably active catalysts will also be discussed.
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spelling pubmed-83057222021-07-25 Direct Arylation in the Presence of Palladium Pincer Complexes Urgoitia, Garazi Herrero, Maria Teresa Churruca, Fátima Conde, Nerea SanMartin, Raul Molecules Review Direct arylation is an atom-economical alternative to more established procedures such as Stille, Suzuki or Negishi arylation reactions. In comparison with other palladium sources and ligands, the use of palladium pincer complexes as catalysts or pre-catalysts for direct arylation has resulted in improved efficiency, higher reaction yields, and advantageous reaction conditions. In addition to a revision of the literature concerning intra- and intermolecular direct arylation reactions performed in the presence of palladium pincer complexes, the role of these remarkably active catalysts will also be discussed. MDPI 2021-07-20 /pmc/articles/PMC8305722/ /pubmed/34299661 http://dx.doi.org/10.3390/molecules26144385 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Urgoitia, Garazi
Herrero, Maria Teresa
Churruca, Fátima
Conde, Nerea
SanMartin, Raul
Direct Arylation in the Presence of Palladium Pincer Complexes
title Direct Arylation in the Presence of Palladium Pincer Complexes
title_full Direct Arylation in the Presence of Palladium Pincer Complexes
title_fullStr Direct Arylation in the Presence of Palladium Pincer Complexes
title_full_unstemmed Direct Arylation in the Presence of Palladium Pincer Complexes
title_short Direct Arylation in the Presence of Palladium Pincer Complexes
title_sort direct arylation in the presence of palladium pincer complexes
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8305722/
https://www.ncbi.nlm.nih.gov/pubmed/34299661
http://dx.doi.org/10.3390/molecules26144385
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