Open Access
Molecules, volume 26, issue 12, pages 3595
Synthesis and reactivity of 3h‐1,2‐dithiole‐3‐thiones
Rakitin Oleg A.
1, 2
Publication type: Journal Article
Publication date: 2021-06-11
PubMed ID:
34208356
Organic Chemistry
Drug Discovery
Physical and Theoretical Chemistry
Pharmaceutical Science
Molecular Medicine
Analytical Chemistry
Chemistry (miscellaneous)
Abstract
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.
Citations by journals
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2
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MolBank
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MolBank
2 publications, 13.33%
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International Journal of Molecular Sciences
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International Journal of Molecular Sciences
2 publications, 13.33%
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Russian Chemical Bulletin
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Russian Chemical Bulletin
1 publication, 6.67%
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Molecules
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Molecules
1 publication, 6.67%
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Biomolecules
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Biomolecules
1 publication, 6.67%
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Materials
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Materials
1 publication, 6.67%
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Journal of Organic Chemistry
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Journal of Organic Chemistry
1 publication, 6.67%
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Journal of Structural Chemistry
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Journal of Structural Chemistry
1 publication, 6.67%
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Journal of Fluorine Chemistry
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Journal of Fluorine Chemistry
1 publication, 6.67%
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Progress in Heterocyclic Chemistry
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Progress in Heterocyclic Chemistry
1 publication, 6.67%
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IUCrData
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IUCrData
1 publication, 6.67%
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Advances in Heterocyclic Chemistry
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Advances in Heterocyclic Chemistry
1 publication, 6.67%
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Journal of Controlled Release
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Journal of Controlled Release
1 publication, 6.67%
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1
2
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Citations by publishers
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7
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Multidisciplinary Digital Publishing Institute (MDPI)
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Multidisciplinary Digital Publishing Institute (MDPI)
7 publications, 46.67%
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Elsevier
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Elsevier
4 publications, 26.67%
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Springer Nature
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Springer Nature
1 publication, 6.67%
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American Chemical Society (ACS)
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American Chemical Society (ACS)
1 publication, 6.67%
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Pleiades Publishing
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Pleiades Publishing
1 publication, 6.67%
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International Union of Crystallography (IUCr)
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International Union of Crystallography (IUCr)
1 publication, 6.67%
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- We do not take into account publications that without a DOI.
- Statistics recalculated only for publications connected to researchers, organizations and labs registered on the platform.
- Statistics recalculated weekly.
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TY - JOUR
DO - 10.3390/molecules26123595
UR - https://doi.org/10.3390%2Fmolecules26123595
TI - Synthesis and reactivity of 3h‐1,2‐dithiole‐3‐thiones
T2 - Molecules
AU - Rakitin, Oleg A.
PY - 2021
DA - 2021/06/11 00:00:00
PB - Multidisciplinary Digital Publishing Institute (MDPI)
SP - 3595
IS - 12
VL - 26
PMID - 34208356
SN - 1420-3049
ER -
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@article{2021_Rakitin
author = {Oleg A. Rakitin},
title = {Synthesis and reactivity of 3h‐1,2‐dithiole‐3‐thiones},
journal = {Molecules},
year = {2021},
volume = {26},
publisher = {Multidisciplinary Digital Publishing Institute (MDPI)},
month = {jun},
url = {https://doi.org/10.3390%2Fmolecules26123595},
number = {12},
pages = {3595},
doi = {10.3390/molecules26123595}
}
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Rakitin, Oleg A.. “Synthesis and reactivity of 3h‐1,2‐dithiole‐3‐thiones.” Molecules, vol. 26, no. 12, Jun. 2021, p. 3595. https://doi.org/10.3390%2Fmolecules26123595.
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