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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....

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Detalles Bibliográficos
Autores principales: Tyrikos-Ergas, Theodore, Sletten, Eric T., Huang, Jhih-Yi, Seeberger, Peter H., Delbianco, Martina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
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.
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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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