Advances in Palladium-Catalyzed Carboxylation Reactions

In this short review, we highlight the advancements in the field of palladium-catalyzed carbon dioxide utilization for the synthesis of high value added organic molecules. The review is structured on the basis of the kind of substrate undergoing the Pd-catalyzed carboxylation process. Accordingly, a...

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Detalles Bibliográficos
Autores principales: Veltri, Lucia, Amuso, Roberta, Mancuso, Raffaella, Gabriele, Bartolo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8746634/
https://www.ncbi.nlm.nih.gov/pubmed/35011494
http://dx.doi.org/10.3390/molecules27010262
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author Veltri, Lucia
Amuso, Roberta
Mancuso, Raffaella
Gabriele, Bartolo
author_facet Veltri, Lucia
Amuso, Roberta
Mancuso, Raffaella
Gabriele, Bartolo
author_sort Veltri, Lucia
collection PubMed
description In this short review, we highlight the advancements in the field of palladium-catalyzed carbon dioxide utilization for the synthesis of high value added organic molecules. The review is structured on the basis of the kind of substrate undergoing the Pd-catalyzed carboxylation process. Accordingly, after the introductory section, the main sections of the review will illustrate Pd-catalyzed carboxylation of olefinic substrates, acetylenic substrates, and other substrates (aryl halides and triflates).
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spelling pubmed-87466342022-01-11 Advances in Palladium-Catalyzed Carboxylation Reactions Veltri, Lucia Amuso, Roberta Mancuso, Raffaella Gabriele, Bartolo Molecules Review In this short review, we highlight the advancements in the field of palladium-catalyzed carbon dioxide utilization for the synthesis of high value added organic molecules. The review is structured on the basis of the kind of substrate undergoing the Pd-catalyzed carboxylation process. Accordingly, after the introductory section, the main sections of the review will illustrate Pd-catalyzed carboxylation of olefinic substrates, acetylenic substrates, and other substrates (aryl halides and triflates). MDPI 2022-01-01 /pmc/articles/PMC8746634/ /pubmed/35011494 http://dx.doi.org/10.3390/molecules27010262 Text en © 2022 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
Veltri, Lucia
Amuso, Roberta
Mancuso, Raffaella
Gabriele, Bartolo
Advances in Palladium-Catalyzed Carboxylation Reactions
title Advances in Palladium-Catalyzed Carboxylation Reactions
title_full Advances in Palladium-Catalyzed Carboxylation Reactions
title_fullStr Advances in Palladium-Catalyzed Carboxylation Reactions
title_full_unstemmed Advances in Palladium-Catalyzed Carboxylation Reactions
title_short Advances in Palladium-Catalyzed Carboxylation Reactions
title_sort advances in palladium-catalyzed carboxylation reactions
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8746634/
https://www.ncbi.nlm.nih.gov/pubmed/35011494
http://dx.doi.org/10.3390/molecules27010262
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AT gabrielebartolo advancesinpalladiumcatalyzedcarboxylationreactions

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