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Investigating radical cation chain processes in the electrocatalytic Diels–Alder reaction

Single electron transfer (SET)-triggered radical ion-based reactions have proven to be powerful options in synthetic organic chemistry. Although unique chain processes have been proposed in various photo- and electrochemical radical ion-based transformations, the turnover number, also referred to as...

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Detalles Bibliográficos
Autores principales: Imada, Yasushi, Okada, Yohei, Chiba, Kazuhiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5870144/
https://www.ncbi.nlm.nih.gov/pubmed/29623126
http://dx.doi.org/10.3762/bjoc.14.51
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author Imada, Yasushi
Okada, Yohei
Chiba, Kazuhiro
author_facet Imada, Yasushi
Okada, Yohei
Chiba, Kazuhiro
author_sort Imada, Yasushi
collection PubMed
description Single electron transfer (SET)-triggered radical ion-based reactions have proven to be powerful options in synthetic organic chemistry. Although unique chain processes have been proposed in various photo- and electrochemical radical ion-based transformations, the turnover number, also referred to as catalytic efficiency, remains unclear in most cases. Herein, we disclose our investigations of radical cation chain processes in the electrocatalytic Diels–Alder reaction, leading to a scalable synthesis. A gram-scale synthesis was achieved with high current efficiency of up to 8000%. The reaction monitoring profiles showed sigmoidal curves with induction periods, suggesting the involvement of intermediate(s) in the rate determining step.
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spelling pubmed-58701442018-04-05 Investigating radical cation chain processes in the electrocatalytic Diels–Alder reaction Imada, Yasushi Okada, Yohei Chiba, Kazuhiro Beilstein J Org Chem Letter Single electron transfer (SET)-triggered radical ion-based reactions have proven to be powerful options in synthetic organic chemistry. Although unique chain processes have been proposed in various photo- and electrochemical radical ion-based transformations, the turnover number, also referred to as catalytic efficiency, remains unclear in most cases. Herein, we disclose our investigations of radical cation chain processes in the electrocatalytic Diels–Alder reaction, leading to a scalable synthesis. A gram-scale synthesis was achieved with high current efficiency of up to 8000%. The reaction monitoring profiles showed sigmoidal curves with induction periods, suggesting the involvement of intermediate(s) in the rate determining step. Beilstein-Institut 2018-03-16 /pmc/articles/PMC5870144/ /pubmed/29623126 http://dx.doi.org/10.3762/bjoc.14.51 Text en Copyright © 2018, Imada et al. https://creativecommons.org/licenses/by/4.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Letter
Imada, Yasushi
Okada, Yohei
Chiba, Kazuhiro
Investigating radical cation chain processes in the electrocatalytic Diels–Alder reaction
title Investigating radical cation chain processes in the electrocatalytic Diels–Alder reaction
title_full Investigating radical cation chain processes in the electrocatalytic Diels–Alder reaction
title_fullStr Investigating radical cation chain processes in the electrocatalytic Diels–Alder reaction
title_full_unstemmed Investigating radical cation chain processes in the electrocatalytic Diels–Alder reaction
title_short Investigating radical cation chain processes in the electrocatalytic Diels–Alder reaction
title_sort investigating radical cation chain processes in the electrocatalytic diels–alder reaction
topic Letter
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5870144/
https://www.ncbi.nlm.nih.gov/pubmed/29623126
http://dx.doi.org/10.3762/bjoc.14.51
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