Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autor principal: Rakitin, Oleg A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
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
_version_ 1783713384179433472
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