Open Access
Synthesis and reactivity of 3h‐1,2‐dithiole‐3‐thiones
Тип публикации: Journal Article
Дата публикации: 2021-06-11
PubMed ID:
34208356
Organic Chemistry
Drug Discovery
Physical and Theoretical Chemistry
Pharmaceutical Science
Molecular Medicine
Analytical Chemistry
Chemistry (miscellaneous)
Краткое описание
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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MLA
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ГОСТ
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Rakitin O. A. Synthesis and reactivity of 3h‐1,2‐dithiole‐3‐thiones // Molecules. 2021. Vol. 26. No. 12. p. 3595.
ГОСТ со всеми авторами (до 50)
Скопировать
Rakitin O. A. Synthesis and reactivity of 3h‐1,2‐dithiole‐3‐thiones // Molecules. 2021. Vol. 26. No. 12. p. 3595.
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RIS
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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 -
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BibTex (до 50 авторов)
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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 = {MDPI},
month = {jun},
url = {https://www.mdpi.com/1420-3049/26/12/3595},
number = {12},
pages = {3595},
doi = {10.3390/molecules26123595}
}
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MLA
Скопировать
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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