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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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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. |
format | Online Article Text |
id | pubmed-8305722 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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