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Synthesis of O-Amino Sugars and Nucleosides
Nucleic acids and carbohydrates are essential biomolecules involved in numerous biological and pathological processes. Development of multifunctional building blocks based on nucleosides and sugars is in high demand for the generation of novel oligonucleotide mimics and glycoconjugates for biomedica...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6017822/ https://www.ncbi.nlm.nih.gov/pubmed/29534554 http://dx.doi.org/10.3390/molecules23030641 |
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author | Chen, Na Xie, Juan |
author_facet | Chen, Na Xie, Juan |
author_sort | Chen, Na |
collection | PubMed |
description | Nucleic acids and carbohydrates are essential biomolecules involved in numerous biological and pathological processes. Development of multifunctional building blocks based on nucleosides and sugars is in high demand for the generation of novel oligonucleotide mimics and glycoconjugates for biomedical applications. Recently, aminooxyl-functionalized compounds have attracted increasing research interest because of their easy derivatization through oxime ligation or N-oxyamide formation reactions. Various biological applications have been reported for O-amino carbohydrate- and nucleoside-derived compounds. Here, we report our efforts in the design and synthesis of glyco-, glycosyl, nucleoside- and nucleo-aminooxy acid derivatives from readily available sugars and amino acids, and their use for the generation of N-oxyamide-linked oligosaccharides, glycopeptides, glycolipids, oligonucleosides and nucleopeptides as novel glycoconjugates or oligonucleotide mimics. Delicate and key points in the synthesis will be emphasized. |
format | Online Article Text |
id | pubmed-6017822 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-60178222018-11-13 Synthesis of O-Amino Sugars and Nucleosides Chen, Na Xie, Juan Molecules Review Nucleic acids and carbohydrates are essential biomolecules involved in numerous biological and pathological processes. Development of multifunctional building blocks based on nucleosides and sugars is in high demand for the generation of novel oligonucleotide mimics and glycoconjugates for biomedical applications. Recently, aminooxyl-functionalized compounds have attracted increasing research interest because of their easy derivatization through oxime ligation or N-oxyamide formation reactions. Various biological applications have been reported for O-amino carbohydrate- and nucleoside-derived compounds. Here, we report our efforts in the design and synthesis of glyco-, glycosyl, nucleoside- and nucleo-aminooxy acid derivatives from readily available sugars and amino acids, and their use for the generation of N-oxyamide-linked oligosaccharides, glycopeptides, glycolipids, oligonucleosides and nucleopeptides as novel glycoconjugates or oligonucleotide mimics. Delicate and key points in the synthesis will be emphasized. MDPI 2018-03-12 /pmc/articles/PMC6017822/ /pubmed/29534554 http://dx.doi.org/10.3390/molecules23030641 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Chen, Na Xie, Juan Synthesis of O-Amino Sugars and Nucleosides |
title | Synthesis of O-Amino Sugars and Nucleosides |
title_full | Synthesis of O-Amino Sugars and Nucleosides |
title_fullStr | Synthesis of O-Amino Sugars and Nucleosides |
title_full_unstemmed | Synthesis of O-Amino Sugars and Nucleosides |
title_short | Synthesis of O-Amino Sugars and Nucleosides |
title_sort | synthesis of o-amino sugars and nucleosides |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6017822/ https://www.ncbi.nlm.nih.gov/pubmed/29534554 http://dx.doi.org/10.3390/molecules23030641 |
work_keys_str_mv | AT chenna synthesisofoaminosugarsandnucleosides AT xiejuan synthesisofoaminosugarsandnucleosides |