Cargando…
Bifunctional dendrons for multiple carbohydrate presentation via carbonyl chemistry
The synthesis of new dendrons of the generations 0, 1 and 2 with a double bond at the focal point and a carbonyl group at the termini has been carried out. The carbonyl group has been exploited for the multivalent conjugation to a sample saccharide by reductive amination and alkoxyamine conjugation.
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4143090/ https://www.ncbi.nlm.nih.gov/pubmed/25161728 http://dx.doi.org/10.3762/bjoc.10.177 |
_version_ | 1782331849959276544 |
---|---|
author | Bini, Davide Nicotra, Francesco Cipolla, Laura |
author_facet | Bini, Davide Nicotra, Francesco Cipolla, Laura |
author_sort | Bini, Davide |
collection | PubMed |
description | The synthesis of new dendrons of the generations 0, 1 and 2 with a double bond at the focal point and a carbonyl group at the termini has been carried out. The carbonyl group has been exploited for the multivalent conjugation to a sample saccharide by reductive amination and alkoxyamine conjugation. |
format | Online Article Text |
id | pubmed-4143090 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-41430902014-08-26 Bifunctional dendrons for multiple carbohydrate presentation via carbonyl chemistry Bini, Davide Nicotra, Francesco Cipolla, Laura Beilstein J Org Chem Letter The synthesis of new dendrons of the generations 0, 1 and 2 with a double bond at the focal point and a carbonyl group at the termini has been carried out. The carbonyl group has been exploited for the multivalent conjugation to a sample saccharide by reductive amination and alkoxyamine conjugation. Beilstein-Institut 2014-07-25 /pmc/articles/PMC4143090/ /pubmed/25161728 http://dx.doi.org/10.3762/bjoc.10.177 Text en Copyright © 2014, Bini et al. 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 | Letter Bini, Davide Nicotra, Francesco Cipolla, Laura Bifunctional dendrons for multiple carbohydrate presentation via carbonyl chemistry |
title | Bifunctional dendrons for multiple carbohydrate presentation via carbonyl chemistry |
title_full | Bifunctional dendrons for multiple carbohydrate presentation via carbonyl chemistry |
title_fullStr | Bifunctional dendrons for multiple carbohydrate presentation via carbonyl chemistry |
title_full_unstemmed | Bifunctional dendrons for multiple carbohydrate presentation via carbonyl chemistry |
title_short | Bifunctional dendrons for multiple carbohydrate presentation via carbonyl chemistry |
title_sort | bifunctional dendrons for multiple carbohydrate presentation via carbonyl chemistry |
topic | Letter |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4143090/ https://www.ncbi.nlm.nih.gov/pubmed/25161728 http://dx.doi.org/10.3762/bjoc.10.177 |
work_keys_str_mv | AT binidavide bifunctionaldendronsformultiplecarbohydratepresentationviacarbonylchemistry AT nicotrafrancesco bifunctionaldendronsformultiplecarbohydratepresentationviacarbonylchemistry AT cipollalaura bifunctionaldendronsformultiplecarbohydratepresentationviacarbonylchemistry |