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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Main Authors: Garazi Urgoitia, Maria Teresa Herrero, Fátima Churruca, Nerea Conde, Raul SanMartin
Format: Article
Language:English
Published: MDPI AG 2021-07-01
Series:Molecules
Subjects:
Online Access:https://www.mdpi.com/1420-3049/26/14/4385
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author Garazi Urgoitia
Maria Teresa Herrero
Fátima Churruca
Nerea Conde
Raul SanMartin
author_facet Garazi Urgoitia
Maria Teresa Herrero
Fátima Churruca
Nerea Conde
Raul SanMartin
author_sort Garazi Urgoitia
collection DOAJ
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 doaj.art-c7cb38a44b294efa804d55ce8b891bec2023-11-22T04:33:03ZengMDPI AGMolecules1420-30492021-07-012614438510.3390/molecules26144385Direct Arylation in the Presence of Palladium Pincer ComplexesGarazi Urgoitia0Maria Teresa Herrero1Fátima Churruca2Nerea Conde3Raul SanMartin4Department of Organic and Inorganic Chemistry, Faculty of Science and Technology, University of the Basque Country (UPV/EHU), 48940 Leioa, SpainDepartment of Organic and Inorganic Chemistry, Faculty of Science and Technology, University of the Basque Country (UPV/EHU), 48940 Leioa, SpainDepartment of Organic and Inorganic Chemistry, Faculty of Science and Technology, University of the Basque Country (UPV/EHU), 48940 Leioa, SpainDepartment of Organic and Inorganic Chemistry, Faculty of Science and Technology, University of the Basque Country (UPV/EHU), 48940 Leioa, SpainDepartment of Organic and Inorganic Chemistry, Faculty of Science and Technology, University of the Basque Country (UPV/EHU), 48940 Leioa, SpainDirect 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.https://www.mdpi.com/1420-3049/26/14/4385direct arylationpalladiumpincer complexes
spellingShingle Garazi Urgoitia
Maria Teresa Herrero
Fátima Churruca
Nerea Conde
Raul SanMartin
Direct Arylation in the Presence of Palladium Pincer Complexes
Molecules
direct arylation
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 direct arylation
palladium
pincer complexes
url https://www.mdpi.com/1420-3049/26/14/4385
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