Electrochemical Synthesis of Sulfinate Esters: Nickel(II)-Catalyzed Oxidative Esterification of Thiols with Alcohols in an Undivided Cell

[Image: see text] In this study, nickel-catalyzed electrochemical oxidative esterification of thiols with alcohols for the synthesis of sulfinate esters has been reported. The electrochemical oxidative esterification proceeded through a nickel-catalyzed oxidation of thiols using an undivided cell of...

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Autores principales: Kaboudin, Babak, Behrouzi, Leila, Kazemi, Foad, Najafpour, Mohammad M., Aoyama, Hiroshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7391255/
https://www.ncbi.nlm.nih.gov/pubmed/32743167
http://dx.doi.org/10.1021/acsomega.0c00953
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author Kaboudin, Babak
Behrouzi, Leila
Kazemi, Foad
Najafpour, Mohammad M.
Aoyama, Hiroshi
author_facet Kaboudin, Babak
Behrouzi, Leila
Kazemi, Foad
Najafpour, Mohammad M.
Aoyama, Hiroshi
author_sort Kaboudin, Babak
collection PubMed
description [Image: see text] In this study, nickel-catalyzed electrochemical oxidative esterification of thiols with alcohols for the synthesis of sulfinate esters has been reported. The electrochemical oxidative esterification proceeded through a nickel-catalyzed oxidation of thiols using an undivided cell of graphite/nickel electrodes, where the nickel oxidation was studied by cyclic voltammetry. The method was conveniently and directly used for the one-pot synthesis of sulfinate esters of thiols.
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spelling pubmed-73912552020-07-31 Electrochemical Synthesis of Sulfinate Esters: Nickel(II)-Catalyzed Oxidative Esterification of Thiols with Alcohols in an Undivided Cell Kaboudin, Babak Behrouzi, Leila Kazemi, Foad Najafpour, Mohammad M. Aoyama, Hiroshi ACS Omega [Image: see text] In this study, nickel-catalyzed electrochemical oxidative esterification of thiols with alcohols for the synthesis of sulfinate esters has been reported. The electrochemical oxidative esterification proceeded through a nickel-catalyzed oxidation of thiols using an undivided cell of graphite/nickel electrodes, where the nickel oxidation was studied by cyclic voltammetry. The method was conveniently and directly used for the one-pot synthesis of sulfinate esters of thiols. American Chemical Society 2020-07-14 /pmc/articles/PMC7391255/ /pubmed/32743167 http://dx.doi.org/10.1021/acsomega.0c00953 Text en Copyright © 2020 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Kaboudin, Babak
Behrouzi, Leila
Kazemi, Foad
Najafpour, Mohammad M.
Aoyama, Hiroshi
Electrochemical Synthesis of Sulfinate Esters: Nickel(II)-Catalyzed Oxidative Esterification of Thiols with Alcohols in an Undivided Cell
title Electrochemical Synthesis of Sulfinate Esters: Nickel(II)-Catalyzed Oxidative Esterification of Thiols with Alcohols in an Undivided Cell
title_full Electrochemical Synthesis of Sulfinate Esters: Nickel(II)-Catalyzed Oxidative Esterification of Thiols with Alcohols in an Undivided Cell
title_fullStr Electrochemical Synthesis of Sulfinate Esters: Nickel(II)-Catalyzed Oxidative Esterification of Thiols with Alcohols in an Undivided Cell
title_full_unstemmed Electrochemical Synthesis of Sulfinate Esters: Nickel(II)-Catalyzed Oxidative Esterification of Thiols with Alcohols in an Undivided Cell
title_short Electrochemical Synthesis of Sulfinate Esters: Nickel(II)-Catalyzed Oxidative Esterification of Thiols with Alcohols in an Undivided Cell
title_sort electrochemical synthesis of sulfinate esters: nickel(ii)-catalyzed oxidative esterification of thiols with alcohols in an undivided cell
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7391255/
https://www.ncbi.nlm.nih.gov/pubmed/32743167
http://dx.doi.org/10.1021/acsomega.0c00953
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