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Direct Synthesis of Unsymmetrical Dithioacetals
Dithioacetals are a frequently used motif in synthetic organic chemistry and have recently seen increasing attention as structural motif in promising antiviral agents against plant pathogens. Most existing reports, however, only discuss symmetrical dithioacetals. Examples of mixed dithioacetals are...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8048688/ https://www.ncbi.nlm.nih.gov/pubmed/33270274 http://dx.doi.org/10.1002/chem.202004835 |
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author | Bognar, Sabine van Gemmeren, Manuel |
author_facet | Bognar, Sabine van Gemmeren, Manuel |
author_sort | Bognar, Sabine |
collection | PubMed |
description | Dithioacetals are a frequently used motif in synthetic organic chemistry and have recently seen increasing attention as structural motif in promising antiviral agents against plant pathogens. Most existing reports, however, only discuss symmetrical dithioacetals. Examples of mixed dithioacetals are scarce and no general method for the selective synthesis of these compounds exists. Herein, a synthetically simple general one‐step protocol was developed for the synthesis of a broad range of unsymmetrical dithioacetals consisting of one aromatic and one aliphatic thiol moiety from the corresponding aldehyde/thiol mixture. The mixed S,S‐acetals were obtained in high yields, and a great variety of functional groups was tolerated. Kinetic control enabled an excellent selectivity in regard to the unsymmetrical dithioacetal. |
format | Online Article Text |
id | pubmed-8048688 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-80486882021-04-19 Direct Synthesis of Unsymmetrical Dithioacetals Bognar, Sabine van Gemmeren, Manuel Chemistry Communications Dithioacetals are a frequently used motif in synthetic organic chemistry and have recently seen increasing attention as structural motif in promising antiviral agents against plant pathogens. Most existing reports, however, only discuss symmetrical dithioacetals. Examples of mixed dithioacetals are scarce and no general method for the selective synthesis of these compounds exists. Herein, a synthetically simple general one‐step protocol was developed for the synthesis of a broad range of unsymmetrical dithioacetals consisting of one aromatic and one aliphatic thiol moiety from the corresponding aldehyde/thiol mixture. The mixed S,S‐acetals were obtained in high yields, and a great variety of functional groups was tolerated. Kinetic control enabled an excellent selectivity in regard to the unsymmetrical dithioacetal. John Wiley and Sons Inc. 2021-01-18 2021-03-12 /pmc/articles/PMC8048688/ /pubmed/33270274 http://dx.doi.org/10.1002/chem.202004835 Text en © 2020 The Authors. Published by Wiley-VCH GmbH https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Communications Bognar, Sabine van Gemmeren, Manuel Direct Synthesis of Unsymmetrical Dithioacetals |
title | Direct Synthesis of Unsymmetrical Dithioacetals |
title_full | Direct Synthesis of Unsymmetrical Dithioacetals |
title_fullStr | Direct Synthesis of Unsymmetrical Dithioacetals |
title_full_unstemmed | Direct Synthesis of Unsymmetrical Dithioacetals |
title_short | Direct Synthesis of Unsymmetrical Dithioacetals |
title_sort | direct synthesis of unsymmetrical dithioacetals |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8048688/ https://www.ncbi.nlm.nih.gov/pubmed/33270274 http://dx.doi.org/10.1002/chem.202004835 |
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