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Synthesis of the pentasaccharide repeating unit of the O-antigen of E. coli O117:K98:H4
The pentasaccharide repeating unit of the O-antigen of E. coli O117:K98:H4 strain has been synthesized using a combination of sequential glycosylations and [3 + 2] block synthetic strategy from the suitably protected monosaccharide intermediates. Thioglycosides and glycosyl trichloroacetimidate deri...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Beilstein-Institut
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4273275/ https://www.ncbi.nlm.nih.gov/pubmed/25550736 http://dx.doi.org/10.3762/bjoc.10.287 |
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author | Mandal, Pintu Kumar |
author_facet | Mandal, Pintu Kumar |
author_sort | Mandal, Pintu Kumar |
collection | PubMed |
description | The pentasaccharide repeating unit of the O-antigen of E. coli O117:K98:H4 strain has been synthesized using a combination of sequential glycosylations and [3 + 2] block synthetic strategy from the suitably protected monosaccharide intermediates. Thioglycosides and glycosyl trichloroacetimidate derivatives have been used as glycosyl donors in the glycosylations. |
format | Online Article Text |
id | pubmed-4273275 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-42732752014-12-30 Synthesis of the pentasaccharide repeating unit of the O-antigen of E. coli O117:K98:H4 Mandal, Pintu Kumar Beilstein J Org Chem Full Research Paper The pentasaccharide repeating unit of the O-antigen of E. coli O117:K98:H4 strain has been synthesized using a combination of sequential glycosylations and [3 + 2] block synthetic strategy from the suitably protected monosaccharide intermediates. Thioglycosides and glycosyl trichloroacetimidate derivatives have been used as glycosyl donors in the glycosylations. Beilstein-Institut 2014-11-20 /pmc/articles/PMC4273275/ /pubmed/25550736 http://dx.doi.org/10.3762/bjoc.10.287 Text en Copyright © 2014, Mandal 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 Mandal, Pintu Kumar Synthesis of the pentasaccharide repeating unit of the O-antigen of E. coli O117:K98:H4 |
title | Synthesis of the pentasaccharide repeating unit of the O-antigen of E. coli O117:K98:H4 |
title_full | Synthesis of the pentasaccharide repeating unit of the O-antigen of E. coli O117:K98:H4 |
title_fullStr | Synthesis of the pentasaccharide repeating unit of the O-antigen of E. coli O117:K98:H4 |
title_full_unstemmed | Synthesis of the pentasaccharide repeating unit of the O-antigen of E. coli O117:K98:H4 |
title_short | Synthesis of the pentasaccharide repeating unit of the O-antigen of E. coli O117:K98:H4 |
title_sort | synthesis of the pentasaccharide repeating unit of the o-antigen of e. coli o117:k98:h4 |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4273275/ https://www.ncbi.nlm.nih.gov/pubmed/25550736 http://dx.doi.org/10.3762/bjoc.10.287 |
work_keys_str_mv | AT mandalpintukumar synthesisofthepentasacchariderepeatingunitoftheoantigenofecolio117k98h4 |