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Synthesis and Reactivity of 3H-1,2-dithiole-3-thiones
3H-1,2-Dithiole-3-thiones are among the best studied classes of polysulfur-containing heterocycles due to the almost explosive recent interest in these compounds as sources of hydrogen sulfide as an endogenously produced gaseous signaling molecule. This review covers the recent developments in the s...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8231234/ https://www.ncbi.nlm.nih.gov/pubmed/34208356 http://dx.doi.org/10.3390/molecules26123595 |
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author | Rakitin, Oleg A. |
author_facet | Rakitin, Oleg A. |
author_sort | Rakitin, Oleg A. |
collection | PubMed |
description | 3H-1,2-Dithiole-3-thiones are among the best studied classes of polysulfur-containing heterocycles due to the almost explosive recent interest in these compounds as sources of hydrogen sulfide as an endogenously produced gaseous signaling molecule. This review covers the recent developments in the synthesis of these heterocycles, including both well-known procedures and important novel transformations for building the 1,2-dithiole-3-thione ring. Diverse ring transformations of 3H-1,2-dithiole-3-thiones into various heterocyclic systems through 1,3-dipolar cycloaddition, replacement of one or two sulfur atoms to form carbon- and carbon-nitrogen containing moieties, and other unexpected reactions are considered. |
format | Online Article Text |
id | pubmed-8231234 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-82312342021-06-26 Synthesis and Reactivity of 3H-1,2-dithiole-3-thiones Rakitin, Oleg A. Molecules Review 3H-1,2-Dithiole-3-thiones are among the best studied classes of polysulfur-containing heterocycles due to the almost explosive recent interest in these compounds as sources of hydrogen sulfide as an endogenously produced gaseous signaling molecule. This review covers the recent developments in the synthesis of these heterocycles, including both well-known procedures and important novel transformations for building the 1,2-dithiole-3-thione ring. Diverse ring transformations of 3H-1,2-dithiole-3-thiones into various heterocyclic systems through 1,3-dipolar cycloaddition, replacement of one or two sulfur atoms to form carbon- and carbon-nitrogen containing moieties, and other unexpected reactions are considered. MDPI 2021-06-11 /pmc/articles/PMC8231234/ /pubmed/34208356 http://dx.doi.org/10.3390/molecules26123595 Text en © 2021 by the author. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Rakitin, Oleg A. Synthesis and Reactivity of 3H-1,2-dithiole-3-thiones |
title | Synthesis and Reactivity of 3H-1,2-dithiole-3-thiones |
title_full | Synthesis and Reactivity of 3H-1,2-dithiole-3-thiones |
title_fullStr | Synthesis and Reactivity of 3H-1,2-dithiole-3-thiones |
title_full_unstemmed | Synthesis and Reactivity of 3H-1,2-dithiole-3-thiones |
title_short | Synthesis and Reactivity of 3H-1,2-dithiole-3-thiones |
title_sort | synthesis and reactivity of 3h-1,2-dithiole-3-thiones |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8231234/ https://www.ncbi.nlm.nih.gov/pubmed/34208356 http://dx.doi.org/10.3390/molecules26123595 |
work_keys_str_mv | AT rakitinolega synthesisandreactivityof3h12dithiole3thiones |