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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...

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Detalles Bibliográficos
Autores principales: Bognar, Sabine, van Gemmeren, Manuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
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.
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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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