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Accessing Gold π-Acid Reactivity under Electrochemical Anode Oxidation (EAO) through Oxidation Relay

The gold π-acid activation under electrochemical condition is achieved for the first time. While EAO allowing easy access to gold(III) intermediates over alternative chemical oxidation under mild conditions, the reported examples so far limited to coupling reactions due to the rapid AuIII reductive...

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Autores principales: Shi, Xiaodong, Zhang, Shuyao, Wei, Jingwen, Ye, Xiaohan, Perez, Angel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Journal Experts 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10350213/
https://www.ncbi.nlm.nih.gov/pubmed/37461542
http://dx.doi.org/10.21203/rs.3.rs-3088453/v1
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author Shi, Xiaodong
Zhang, Shuyao
Wei, Jingwen
Ye, Xiaohan
Perez, Angel
author_facet Shi, Xiaodong
Zhang, Shuyao
Wei, Jingwen
Ye, Xiaohan
Perez, Angel
author_sort Shi, Xiaodong
collection PubMed
description The gold π-acid activation under electrochemical condition is achieved for the first time. While EAO allowing easy access to gold(III) intermediates over alternative chemical oxidation under mild conditions, the reported examples so far limited to coupling reactions due to the rapid AuIII reductive elimination. Using aryl hydrazine-HOTf salt as precursors, the π-activation reaction mode was realized through oxidation relay. Both alkene and alkyne di-functionalization were achieved with excellent functional group compatibility and regioselectivity, which extended the versatility and utility of electrochemical gold redox chemistry for future applications to come.
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spelling pubmed-103502132023-07-17 Accessing Gold π-Acid Reactivity under Electrochemical Anode Oxidation (EAO) through Oxidation Relay Shi, Xiaodong Zhang, Shuyao Wei, Jingwen Ye, Xiaohan Perez, Angel Res Sq Article The gold π-acid activation under electrochemical condition is achieved for the first time. While EAO allowing easy access to gold(III) intermediates over alternative chemical oxidation under mild conditions, the reported examples so far limited to coupling reactions due to the rapid AuIII reductive elimination. Using aryl hydrazine-HOTf salt as precursors, the π-activation reaction mode was realized through oxidation relay. Both alkene and alkyne di-functionalization were achieved with excellent functional group compatibility and regioselectivity, which extended the versatility and utility of electrochemical gold redox chemistry for future applications to come. American Journal Experts 2023-07-07 /pmc/articles/PMC10350213/ /pubmed/37461542 http://dx.doi.org/10.21203/rs.3.rs-3088453/v1 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use.
spellingShingle Article
Shi, Xiaodong
Zhang, Shuyao
Wei, Jingwen
Ye, Xiaohan
Perez, Angel
Accessing Gold π-Acid Reactivity under Electrochemical Anode Oxidation (EAO) through Oxidation Relay
title Accessing Gold π-Acid Reactivity under Electrochemical Anode Oxidation (EAO) through Oxidation Relay
title_full Accessing Gold π-Acid Reactivity under Electrochemical Anode Oxidation (EAO) through Oxidation Relay
title_fullStr Accessing Gold π-Acid Reactivity under Electrochemical Anode Oxidation (EAO) through Oxidation Relay
title_full_unstemmed Accessing Gold π-Acid Reactivity under Electrochemical Anode Oxidation (EAO) through Oxidation Relay
title_short Accessing Gold π-Acid Reactivity under Electrochemical Anode Oxidation (EAO) through Oxidation Relay
title_sort accessing gold π-acid reactivity under electrochemical anode oxidation (eao) through oxidation relay
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10350213/
https://www.ncbi.nlm.nih.gov/pubmed/37461542
http://dx.doi.org/10.21203/rs.3.rs-3088453/v1
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