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O(2)-Mediated Te(II)-Redox Catalysis for the Cross-Dehydrogenative Coupling of Indoles

[Image: see text] Very few elements in the periodic system can catalytically activate O(2), such as in the context of cross-dehydrogenative couplings. The development of O(2)-activating catalysts is essential to enable new and sustainable reactivity concepts to emerge, because these catalysts also o...

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Autores principales: Cremer, Christopher, Patureau, Frederic W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9241012/
https://www.ncbi.nlm.nih.gov/pubmed/35783164
http://dx.doi.org/10.1021/jacsau.2c00193
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author Cremer, Christopher
Patureau, Frederic W.
author_facet Cremer, Christopher
Patureau, Frederic W.
author_sort Cremer, Christopher
collection PubMed
description [Image: see text] Very few elements in the periodic system can catalytically activate O(2), such as in the context of cross-dehydrogenative couplings. The development of O(2)-activating catalysts is essential to enable new and sustainable reactivity concepts to emerge, because these catalysts also often feature specific activating interactions with the target substrates. In this context, the unprecedented Te(II)/Te(III) catalyzed dehydrogenative C3–C2 dimerization of indoles is described herein. The fact that O(2) can be directly utilized as a terminal oxidant in this reaction, as well as the absence of any background reactivity without the redox-active Te catalyst, constitute very important milestones for the fields of cross-dehydrogenative couplings and tellurium catalysis.
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spelling pubmed-92410122022-06-30 O(2)-Mediated Te(II)-Redox Catalysis for the Cross-Dehydrogenative Coupling of Indoles Cremer, Christopher Patureau, Frederic W. JACS Au [Image: see text] Very few elements in the periodic system can catalytically activate O(2), such as in the context of cross-dehydrogenative couplings. The development of O(2)-activating catalysts is essential to enable new and sustainable reactivity concepts to emerge, because these catalysts also often feature specific activating interactions with the target substrates. In this context, the unprecedented Te(II)/Te(III) catalyzed dehydrogenative C3–C2 dimerization of indoles is described herein. The fact that O(2) can be directly utilized as a terminal oxidant in this reaction, as well as the absence of any background reactivity without the redox-active Te catalyst, constitute very important milestones for the fields of cross-dehydrogenative couplings and tellurium catalysis. American Chemical Society 2022-06-16 /pmc/articles/PMC9241012/ /pubmed/35783164 http://dx.doi.org/10.1021/jacsau.2c00193 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Cremer, Christopher
Patureau, Frederic W.
O(2)-Mediated Te(II)-Redox Catalysis for the Cross-Dehydrogenative Coupling of Indoles
title O(2)-Mediated Te(II)-Redox Catalysis for the Cross-Dehydrogenative Coupling of Indoles
title_full O(2)-Mediated Te(II)-Redox Catalysis for the Cross-Dehydrogenative Coupling of Indoles
title_fullStr O(2)-Mediated Te(II)-Redox Catalysis for the Cross-Dehydrogenative Coupling of Indoles
title_full_unstemmed O(2)-Mediated Te(II)-Redox Catalysis for the Cross-Dehydrogenative Coupling of Indoles
title_short O(2)-Mediated Te(II)-Redox Catalysis for the Cross-Dehydrogenative Coupling of Indoles
title_sort o(2)-mediated te(ii)-redox catalysis for the cross-dehydrogenative coupling of indoles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9241012/
https://www.ncbi.nlm.nih.gov/pubmed/35783164
http://dx.doi.org/10.1021/jacsau.2c00193
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