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Pd(II)-catalyzed carboxylation of aromatic C─H bonds with CO(2)

The carboxylation of nonactivated C─H bonds provides an attractive yet hitherto largely elusive chemical process to synthesize carboxylic acids by incorporation of CO(2) into the chemical value chain. Here, we report on the realization of such a reaction using simple and nonactivated arenes as start...

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Autores principales: Kemper, Gregor, Hölscher, Markus, Leitner, Walter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9897662/
https://www.ncbi.nlm.nih.gov/pubmed/36735781
http://dx.doi.org/10.1126/sciadv.adf2966
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author Kemper, Gregor
Hölscher, Markus
Leitner, Walter
author_facet Kemper, Gregor
Hölscher, Markus
Leitner, Walter
author_sort Kemper, Gregor
collection PubMed
description The carboxylation of nonactivated C─H bonds provides an attractive yet hitherto largely elusive chemical process to synthesize carboxylic acids by incorporation of CO(2) into the chemical value chain. Here, we report on the realization of such a reaction using simple and nonactivated arenes as starting materials. A computationally designed Pd(II) complex acts as organometallic single-component catalyst, and apart from a base, necessary for thermodynamic stabilization of the intermediates, no other additives or coreagents are required. Turnover numbers up to 10(2) and high regioselectivities are achieved. The potential of this catalytic reaction for “green chemistry” is demonstrated by the synthesis of veratric acid, an intermediate for pharmaceutical production, from CO(2) and veratrol.
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spelling pubmed-98976622023-02-08 Pd(II)-catalyzed carboxylation of aromatic C─H bonds with CO(2) Kemper, Gregor Hölscher, Markus Leitner, Walter Sci Adv Physical and Materials Sciences The carboxylation of nonactivated C─H bonds provides an attractive yet hitherto largely elusive chemical process to synthesize carboxylic acids by incorporation of CO(2) into the chemical value chain. Here, we report on the realization of such a reaction using simple and nonactivated arenes as starting materials. A computationally designed Pd(II) complex acts as organometallic single-component catalyst, and apart from a base, necessary for thermodynamic stabilization of the intermediates, no other additives or coreagents are required. Turnover numbers up to 10(2) and high regioselectivities are achieved. The potential of this catalytic reaction for “green chemistry” is demonstrated by the synthesis of veratric acid, an intermediate for pharmaceutical production, from CO(2) and veratrol. American Association for the Advancement of Science 2023-02-03 /pmc/articles/PMC9897662/ /pubmed/36735781 http://dx.doi.org/10.1126/sciadv.adf2966 Text en Copyright © 2023 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Physical and Materials Sciences
Kemper, Gregor
Hölscher, Markus
Leitner, Walter
Pd(II)-catalyzed carboxylation of aromatic C─H bonds with CO(2)
title Pd(II)-catalyzed carboxylation of aromatic C─H bonds with CO(2)
title_full Pd(II)-catalyzed carboxylation of aromatic C─H bonds with CO(2)
title_fullStr Pd(II)-catalyzed carboxylation of aromatic C─H bonds with CO(2)
title_full_unstemmed Pd(II)-catalyzed carboxylation of aromatic C─H bonds with CO(2)
title_short Pd(II)-catalyzed carboxylation of aromatic C─H bonds with CO(2)
title_sort pd(ii)-catalyzed carboxylation of aromatic c─h bonds with co(2)
topic Physical and Materials Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9897662/
https://www.ncbi.nlm.nih.gov/pubmed/36735781
http://dx.doi.org/10.1126/sciadv.adf2966
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