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Synthesis of aryl cyclopropyl sulfides through copper-promoted S-cyclopropylation of thiophenols using cyclopropylboronic acid

The copper-promoted S-cyclopropylation of thiophenols using cyclopropylboronic acid is reported. The procedure operates under simple conditions to afford the corresponding aryl cyclopropyl sulfides in moderate to excellent yields. The reaction tolerates substitution in ortho-, meta- and para-substit...

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Detalles Bibliográficos
Autores principales: Benoit, Emeline, Fnaiche, Ahmed, Gagnon, Alexandre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6604732/
https://www.ncbi.nlm.nih.gov/pubmed/31293663
http://dx.doi.org/10.3762/bjoc.15.113
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author Benoit, Emeline
Fnaiche, Ahmed
Gagnon, Alexandre
author_facet Benoit, Emeline
Fnaiche, Ahmed
Gagnon, Alexandre
author_sort Benoit, Emeline
collection PubMed
description The copper-promoted S-cyclopropylation of thiophenols using cyclopropylboronic acid is reported. The procedure operates under simple conditions to afford the corresponding aryl cyclopropyl sulfides in moderate to excellent yields. The reaction tolerates substitution in ortho-, meta- and para-substitution as well as electron-donating and electron-withdrawing groups. The S-cyclopropylation of a thiophenol was also accomplished using potassium cyclopropyl trifluoroborate.
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spelling pubmed-66047322019-07-10 Synthesis of aryl cyclopropyl sulfides through copper-promoted S-cyclopropylation of thiophenols using cyclopropylboronic acid Benoit, Emeline Fnaiche, Ahmed Gagnon, Alexandre Beilstein J Org Chem Letter The copper-promoted S-cyclopropylation of thiophenols using cyclopropylboronic acid is reported. The procedure operates under simple conditions to afford the corresponding aryl cyclopropyl sulfides in moderate to excellent yields. The reaction tolerates substitution in ortho-, meta- and para-substitution as well as electron-donating and electron-withdrawing groups. The S-cyclopropylation of a thiophenol was also accomplished using potassium cyclopropyl trifluoroborate. Beilstein-Institut 2019-05-27 /pmc/articles/PMC6604732/ /pubmed/31293663 http://dx.doi.org/10.3762/bjoc.15.113 Text en Copyright © 2019, Benoit 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). Please note that the reuse, redistribution and reproduction in particular requires that the authors and source are credited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Letter
Benoit, Emeline
Fnaiche, Ahmed
Gagnon, Alexandre
Synthesis of aryl cyclopropyl sulfides through copper-promoted S-cyclopropylation of thiophenols using cyclopropylboronic acid
title Synthesis of aryl cyclopropyl sulfides through copper-promoted S-cyclopropylation of thiophenols using cyclopropylboronic acid
title_full Synthesis of aryl cyclopropyl sulfides through copper-promoted S-cyclopropylation of thiophenols using cyclopropylboronic acid
title_fullStr Synthesis of aryl cyclopropyl sulfides through copper-promoted S-cyclopropylation of thiophenols using cyclopropylboronic acid
title_full_unstemmed Synthesis of aryl cyclopropyl sulfides through copper-promoted S-cyclopropylation of thiophenols using cyclopropylboronic acid
title_short Synthesis of aryl cyclopropyl sulfides through copper-promoted S-cyclopropylation of thiophenols using cyclopropylboronic acid
title_sort synthesis of aryl cyclopropyl sulfides through copper-promoted s-cyclopropylation of thiophenols using cyclopropylboronic acid
topic Letter
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6604732/
https://www.ncbi.nlm.nih.gov/pubmed/31293663
http://dx.doi.org/10.3762/bjoc.15.113
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