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On resin synthesis of sulfated oligosaccharides
Sulfated glycans are involved in many biological processes, making well-defined sulfated oligosaccharides highly sought molecular probes. These compounds are a considerable synthetic challenge, with each oligosaccharide target requiring specific synthetic protocols and extensive purifications steps....
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8848854/ https://www.ncbi.nlm.nih.gov/pubmed/35308866 http://dx.doi.org/10.1039/d1sc06063e |
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author | Tyrikos-Ergas, Theodore Sletten, Eric T. Huang, Jhih-Yi Seeberger, Peter H. Delbianco, Martina |
author_facet | Tyrikos-Ergas, Theodore Sletten, Eric T. Huang, Jhih-Yi Seeberger, Peter H. Delbianco, Martina |
author_sort | Tyrikos-Ergas, Theodore |
collection | PubMed |
description | Sulfated glycans are involved in many biological processes, making well-defined sulfated oligosaccharides highly sought molecular probes. These compounds are a considerable synthetic challenge, with each oligosaccharide target requiring specific synthetic protocols and extensive purifications steps. Here, we describe a general on resin approach that simplifies the synthesis of sulfated glycans. The oligosaccharide backbone, obtained by Automated Glycan Assembly (AGA), is subjected to regioselective sulfation and hydrolysis of protecting groups. The protocol is compatible with several monosaccharides and allows for multi-sulfation of linear and branched glycans. Seven diverse, biologically relevant sulfated glycans were prepared in good to excellent overall yield. |
format | Online Article Text |
id | pubmed-8848854 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-88488542022-03-17 On resin synthesis of sulfated oligosaccharides Tyrikos-Ergas, Theodore Sletten, Eric T. Huang, Jhih-Yi Seeberger, Peter H. Delbianco, Martina Chem Sci Chemistry Sulfated glycans are involved in many biological processes, making well-defined sulfated oligosaccharides highly sought molecular probes. These compounds are a considerable synthetic challenge, with each oligosaccharide target requiring specific synthetic protocols and extensive purifications steps. Here, we describe a general on resin approach that simplifies the synthesis of sulfated glycans. The oligosaccharide backbone, obtained by Automated Glycan Assembly (AGA), is subjected to regioselective sulfation and hydrolysis of protecting groups. The protocol is compatible with several monosaccharides and allows for multi-sulfation of linear and branched glycans. Seven diverse, biologically relevant sulfated glycans were prepared in good to excellent overall yield. The Royal Society of Chemistry 2022-01-31 /pmc/articles/PMC8848854/ /pubmed/35308866 http://dx.doi.org/10.1039/d1sc06063e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Tyrikos-Ergas, Theodore Sletten, Eric T. Huang, Jhih-Yi Seeberger, Peter H. Delbianco, Martina On resin synthesis of sulfated oligosaccharides |
title | On resin synthesis of sulfated oligosaccharides |
title_full | On resin synthesis of sulfated oligosaccharides |
title_fullStr | On resin synthesis of sulfated oligosaccharides |
title_full_unstemmed | On resin synthesis of sulfated oligosaccharides |
title_short | On resin synthesis of sulfated oligosaccharides |
title_sort | on resin synthesis of sulfated oligosaccharides |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8848854/ https://www.ncbi.nlm.nih.gov/pubmed/35308866 http://dx.doi.org/10.1039/d1sc06063e |
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