Open Access
Synthesis and reactivity of 3h‐1,2‐dithiole‐3‐thiones
Oleg A. Rakitin
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.
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21
Total citations:
21
Citations from 2024:
10
(47%)
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MLA
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RIS
Copy
TY - JOUR
DO - 10.3390/molecules26123595
UR - https://www.mdpi.com/1420-3049/26/12/3595
TI - Synthesis and reactivity of 3h‐1,2‐dithiole‐3‐thiones
T2 - Molecules
AU - Rakitin, Oleg A.
PY - 2021
DA - 2021/06/11
PB - MDPI
SP - 3595
IS - 12
VL - 26
PMID - 34208356
SN - 1420-3049
ER -
Cite this
BibTex (up to 50 authors)
Copy
@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 = {MDPI},
month = {jun},
url = {https://www.mdpi.com/1420-3049/26/12/3595},
number = {12},
pages = {3595},
doi = {10.3390/molecules26123595}
}
Cite this
MLA
Copy
Rakitin, Oleg A.. “Synthesis and reactivity of 3h‐1,2‐dithiole‐3‐thiones.” Molecules, vol. 26, no. 12, Jun. 2021, p. 3595. https://www.mdpi.com/1420-3049/26/12/3595.
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