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β-Hydroxy sulfides and their syntheses

Sulfur-containing natural products are ubiquitous in nature, their most abundant source being marine organisms since sulfur, in the form of the sulfate ion, is the second most abundant anion in sea water after chloride. As part of natural products, sulfur can appear in a multitude of combinations an...

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Detalles Bibliográficos
Autores principales: Marakalala, Mokgethwa Bruce, Mmutlane, Edwin M, Kinfe, Henok H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6036969/
https://www.ncbi.nlm.nih.gov/pubmed/30013693
http://dx.doi.org/10.3762/bjoc.14.143
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author Marakalala, Mokgethwa Bruce
Mmutlane, Edwin M
Kinfe, Henok H
author_facet Marakalala, Mokgethwa Bruce
Mmutlane, Edwin M
Kinfe, Henok H
author_sort Marakalala, Mokgethwa Bruce
collection PubMed
description Sulfur-containing natural products are ubiquitous in nature, their most abundant source being marine organisms since sulfur, in the form of the sulfate ion, is the second most abundant anion in sea water after chloride. As part of natural products, sulfur can appear in a multitude of combinations and oxidation states: thiol, sulfide (acyclic or heterocyclic), disulfide, sulfoxide, sulfonate, thioaminal, hemithioacetal, various thioesters, thiocarbamate and isothiocyanate. This review article focuses on β-hydroxy sulfides and analogs; their presence in natural products, general protocols for their synthesis, and examples of their application in target oriented synthesis.
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spelling pubmed-60369692018-07-16 β-Hydroxy sulfides and their syntheses Marakalala, Mokgethwa Bruce Mmutlane, Edwin M Kinfe, Henok H Beilstein J Org Chem Review Sulfur-containing natural products are ubiquitous in nature, their most abundant source being marine organisms since sulfur, in the form of the sulfate ion, is the second most abundant anion in sea water after chloride. As part of natural products, sulfur can appear in a multitude of combinations and oxidation states: thiol, sulfide (acyclic or heterocyclic), disulfide, sulfoxide, sulfonate, thioaminal, hemithioacetal, various thioesters, thiocarbamate and isothiocyanate. This review article focuses on β-hydroxy sulfides and analogs; their presence in natural products, general protocols for their synthesis, and examples of their application in target oriented synthesis. Beilstein-Institut 2018-07-05 /pmc/articles/PMC6036969/ /pubmed/30013693 http://dx.doi.org/10.3762/bjoc.14.143 Text en Copyright © 2018, Marakalala et al. https://creativecommons.org/licenses/by/4.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Review
Marakalala, Mokgethwa Bruce
Mmutlane, Edwin M
Kinfe, Henok H
β-Hydroxy sulfides and their syntheses
title β-Hydroxy sulfides and their syntheses
title_full β-Hydroxy sulfides and their syntheses
title_fullStr β-Hydroxy sulfides and their syntheses
title_full_unstemmed β-Hydroxy sulfides and their syntheses
title_short β-Hydroxy sulfides and their syntheses
title_sort β-hydroxy sulfides and their syntheses
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6036969/
https://www.ncbi.nlm.nih.gov/pubmed/30013693
http://dx.doi.org/10.3762/bjoc.14.143
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