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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2019
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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. |
format | Online Article Text |
id | pubmed-6604732 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
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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