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The Synthesis and Glycoside Formation of Polyfluorinated Carbohydrates
[Image: see text] Fluorinated carbohydrates have found many applications in the glycosciences. Typically, these contain fluorination at a single position. There are not many applications involving polyfluorinated carbohydrates, here defined as monosaccharides in which more than one carbon has at lea...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9615045/ https://www.ncbi.nlm.nih.gov/pubmed/35613331 http://dx.doi.org/10.1021/acs.chemrev.2c00086 |
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author | Huonnic, Kler Linclau, Bruno |
author_facet | Huonnic, Kler Linclau, Bruno |
author_sort | Huonnic, Kler |
collection | PubMed |
description | [Image: see text] Fluorinated carbohydrates have found many applications in the glycosciences. Typically, these contain fluorination at a single position. There are not many applications involving polyfluorinated carbohydrates, here defined as monosaccharides in which more than one carbon has at least one fluorine substituent directly attached to it, with the notable exception of their use as mechanism-based inhibitors. The increasing attention to carbohydrate physical properties, especially around lipophilicity, has resulted in a surge of interest for this class of compounds. This review covers the considerable body of work toward the synthesis of polyfluorinated hexoses, pentoses, ketosugars, and aminosugars including sialic acids and nucleosides. An overview of the current state of the art of their glycosidation is also provided. |
format | Online Article Text |
id | pubmed-9615045 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-96150452022-10-29 The Synthesis and Glycoside Formation of Polyfluorinated Carbohydrates Huonnic, Kler Linclau, Bruno Chem Rev [Image: see text] Fluorinated carbohydrates have found many applications in the glycosciences. Typically, these contain fluorination at a single position. There are not many applications involving polyfluorinated carbohydrates, here defined as monosaccharides in which more than one carbon has at least one fluorine substituent directly attached to it, with the notable exception of their use as mechanism-based inhibitors. The increasing attention to carbohydrate physical properties, especially around lipophilicity, has resulted in a surge of interest for this class of compounds. This review covers the considerable body of work toward the synthesis of polyfluorinated hexoses, pentoses, ketosugars, and aminosugars including sialic acids and nucleosides. An overview of the current state of the art of their glycosidation is also provided. American Chemical Society 2022-05-25 2022-10-26 /pmc/articles/PMC9615045/ /pubmed/35613331 http://dx.doi.org/10.1021/acs.chemrev.2c00086 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Huonnic, Kler Linclau, Bruno The Synthesis and Glycoside Formation of Polyfluorinated Carbohydrates |
title | The Synthesis and Glycoside Formation of Polyfluorinated
Carbohydrates |
title_full | The Synthesis and Glycoside Formation of Polyfluorinated
Carbohydrates |
title_fullStr | The Synthesis and Glycoside Formation of Polyfluorinated
Carbohydrates |
title_full_unstemmed | The Synthesis and Glycoside Formation of Polyfluorinated
Carbohydrates |
title_short | The Synthesis and Glycoside Formation of Polyfluorinated
Carbohydrates |
title_sort | synthesis and glycoside formation of polyfluorinated
carbohydrates |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9615045/ https://www.ncbi.nlm.nih.gov/pubmed/35613331 http://dx.doi.org/10.1021/acs.chemrev.2c00086 |
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