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Synthesis of aromatic glycoconjugates. Building blocks for the construction of combinatorial glycopeptide libraries
New aromatic glycoconjugate building blocks based on the trifunctional 3-aminomethyl-5-aminobenzoic acid backbone and sugars linked to the backbone by a malonyl moiety were prepared via peptide coupling. The orthogonally protected glycoconjugates, bearing an acetyl-protected glycoside, were converte...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4222372/ https://www.ncbi.nlm.nih.gov/pubmed/25383116 http://dx.doi.org/10.3762/bjoc.10.256 |
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author | Nörrlinger, Markus Ziegler, Thomas |
author_facet | Nörrlinger, Markus Ziegler, Thomas |
author_sort | Nörrlinger, Markus |
collection | PubMed |
description | New aromatic glycoconjugate building blocks based on the trifunctional 3-aminomethyl-5-aminobenzoic acid backbone and sugars linked to the backbone by a malonyl moiety were prepared via peptide coupling. The orthogonally protected glycoconjugates, bearing an acetyl-protected glycoside, were converted into their corresponding acids which are suitable building blocks for combinatorial glycopeptide synthesis. |
format | Online Article Text |
id | pubmed-4222372 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-42223722014-11-07 Synthesis of aromatic glycoconjugates. Building blocks for the construction of combinatorial glycopeptide libraries Nörrlinger, Markus Ziegler, Thomas Beilstein J Org Chem Full Research Paper New aromatic glycoconjugate building blocks based on the trifunctional 3-aminomethyl-5-aminobenzoic acid backbone and sugars linked to the backbone by a malonyl moiety were prepared via peptide coupling. The orthogonally protected glycoconjugates, bearing an acetyl-protected glycoside, were converted into their corresponding acids which are suitable building blocks for combinatorial glycopeptide synthesis. Beilstein-Institut 2014-10-22 /pmc/articles/PMC4222372/ /pubmed/25383116 http://dx.doi.org/10.3762/bjoc.10.256 Text en Copyright © 2014, Nörrlinger and Ziegler https://creativecommons.org/licenses/by/2.0https://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/2.0), 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 | Full Research Paper Nörrlinger, Markus Ziegler, Thomas Synthesis of aromatic glycoconjugates. Building blocks for the construction of combinatorial glycopeptide libraries |
title | Synthesis of aromatic glycoconjugates. Building blocks for the construction of combinatorial glycopeptide libraries |
title_full | Synthesis of aromatic glycoconjugates. Building blocks for the construction of combinatorial glycopeptide libraries |
title_fullStr | Synthesis of aromatic glycoconjugates. Building blocks for the construction of combinatorial glycopeptide libraries |
title_full_unstemmed | Synthesis of aromatic glycoconjugates. Building blocks for the construction of combinatorial glycopeptide libraries |
title_short | Synthesis of aromatic glycoconjugates. Building blocks for the construction of combinatorial glycopeptide libraries |
title_sort | synthesis of aromatic glycoconjugates. building blocks for the construction of combinatorial glycopeptide libraries |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4222372/ https://www.ncbi.nlm.nih.gov/pubmed/25383116 http://dx.doi.org/10.3762/bjoc.10.256 |
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