Chemistry of Substituted Thiazinanes and Their Derivatives

Thiazinanes and its isomeric forms represent one of the most important heterocyclic compounds, and their derivatives represented a highly potent drug in disease treatment such as, 1,1-dioxido-1,2-thiazinan-1,6-naphthyridine, which has been shown to have anti-HIV activity by a mechanism that should w...

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Main Authors: Alaa A. Hassan, Stefan Bräse, Ashraf A. Aly, Hendawy N. Tawfeek
Format: Article
Language:English
Published: MDPI AG 2020-11-01
Series:Molecules
Subjects:
Online Access:https://www.mdpi.com/1420-3049/25/23/5610
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author Alaa A. Hassan
Stefan Bräse
Ashraf A. Aly
Hendawy N. Tawfeek
author_facet Alaa A. Hassan
Stefan Bräse
Ashraf A. Aly
Hendawy N. Tawfeek
author_sort Alaa A. Hassan
collection DOAJ
description Thiazinanes and its isomeric forms represent one of the most important heterocyclic compounds, and their derivatives represented a highly potent drug in disease treatment such as, 1,1-dioxido-1,2-thiazinan-1,6-naphthyridine, which has been shown to have anti-HIV activity by a mechanism that should work as anti-AIDS treatment, while (<i>Z</i>)-methyl 3-(naphthalen-1-ylimino)- 2-thia-4-azaspiro[5 5]undecane-4-carbodithioate showed analgesic activity, cephradine was used as antibiotic and chlormezanone was utilized as anticoagulants. All publications were interested in the chemistry of thiazine (partially or fully unsaturated heterocyclic six-membered ring containing nitrogen and sulfur), but no one was dealing with thiazinane itself which encouraged us to shed new light on these interesting heterocycles. This review was focused on the synthetic approaches of thiazinane derivatives and their chemical reactivity.
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spelling doaj.art-3d6169ddce4c4f419bd3fdb7856accf02023-11-20T22:47:13ZengMDPI AGMolecules1420-30492020-11-012523561010.3390/molecules25235610Chemistry of Substituted Thiazinanes and Their DerivativesAlaa A. Hassan0Stefan Bräse1Ashraf A. Aly2Hendawy N. Tawfeek3Chemistry Department, Faculty of Science, Minia University, El-Minia 61519, EgyptInstitute of Organic Chemistry, Karlsruhe Institute of Technology, 76131 Karlsruhe, GermanyChemistry Department, Faculty of Science, Minia University, El-Minia 61519, EgyptChemistry Department, Faculty of Science, Minia University, El-Minia 61519, EgyptThiazinanes and its isomeric forms represent one of the most important heterocyclic compounds, and their derivatives represented a highly potent drug in disease treatment such as, 1,1-dioxido-1,2-thiazinan-1,6-naphthyridine, which has been shown to have anti-HIV activity by a mechanism that should work as anti-AIDS treatment, while (<i>Z</i>)-methyl 3-(naphthalen-1-ylimino)- 2-thia-4-azaspiro[5 5]undecane-4-carbodithioate showed analgesic activity, cephradine was used as antibiotic and chlormezanone was utilized as anticoagulants. All publications were interested in the chemistry of thiazine (partially or fully unsaturated heterocyclic six-membered ring containing nitrogen and sulfur), but no one was dealing with thiazinane itself which encouraged us to shed new light on these interesting heterocycles. This review was focused on the synthetic approaches of thiazinane derivatives and their chemical reactivity.https://www.mdpi.com/1420-3049/25/23/5610biologic activityfused-heterocyclesspiro compoundsstructuresthiazinanes
spellingShingle Alaa A. Hassan
Stefan Bräse
Ashraf A. Aly
Hendawy N. Tawfeek
Chemistry of Substituted Thiazinanes and Their Derivatives
Molecules
biologic activity
fused-heterocycles
spiro compounds
structures
thiazinanes
title Chemistry of Substituted Thiazinanes and Their Derivatives
title_full Chemistry of Substituted Thiazinanes and Their Derivatives
title_fullStr Chemistry of Substituted Thiazinanes and Their Derivatives
title_full_unstemmed Chemistry of Substituted Thiazinanes and Their Derivatives
title_short Chemistry of Substituted Thiazinanes and Their Derivatives
title_sort chemistry of substituted thiazinanes and their derivatives
topic biologic activity
fused-heterocycles
spiro compounds
structures
thiazinanes
url https://www.mdpi.com/1420-3049/25/23/5610
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