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Easy access to a carbohydrate-based template for stimuli-responsive surfactants

In this paper we describe the synthesis of a new carbohydrate-based building block functionalized with azido or amino groups on the 2 and 4 positions. The building block can be synthesized in anomerically pure form in only five scalable steps starting from commercially available levoglucosan. It was...

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Detalles Bibliográficos
Autores principales: Holmstrøm, Thomas, Raydan, Daniel, Pedersen, Christian Marcus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7684687/
https://www.ncbi.nlm.nih.gov/pubmed/33281982
http://dx.doi.org/10.3762/bjoc.16.229
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author Holmstrøm, Thomas
Raydan, Daniel
Pedersen, Christian Marcus
author_facet Holmstrøm, Thomas
Raydan, Daniel
Pedersen, Christian Marcus
author_sort Holmstrøm, Thomas
collection PubMed
description In this paper we describe the synthesis of a new carbohydrate-based building block functionalized with azido or amino groups on the 2 and 4 positions. The building block can be synthesized in anomerically pure form in only five scalable steps starting from commercially available levoglucosan. It was shown that the building block could undergo alkylations under strongly basic conditions. The building block with azido groups could furthermore take part in CuAAC reactions, generating derivatives with ester or carboxylic acid functionalities. In addition, the anomeric mixture of the building block was used for the synthesis of a molecule that could act as an emulsifier only in the presence of Zn(2+) ions.
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spelling pubmed-76846872020-12-04 Easy access to a carbohydrate-based template for stimuli-responsive surfactants Holmstrøm, Thomas Raydan, Daniel Pedersen, Christian Marcus Beilstein J Org Chem Full Research Paper In this paper we describe the synthesis of a new carbohydrate-based building block functionalized with azido or amino groups on the 2 and 4 positions. The building block can be synthesized in anomerically pure form in only five scalable steps starting from commercially available levoglucosan. It was shown that the building block could undergo alkylations under strongly basic conditions. The building block with azido groups could furthermore take part in CuAAC reactions, generating derivatives with ester or carboxylic acid functionalities. In addition, the anomeric mixture of the building block was used for the synthesis of a molecule that could act as an emulsifier only in the presence of Zn(2+) ions. Beilstein-Institut 2020-11-17 /pmc/articles/PMC7684687/ /pubmed/33281982 http://dx.doi.org/10.3762/bjoc.16.229 Text en Copyright © 2020, Holmstrøm et al. https://creativecommons.org/licenses/by/4.0https://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/4.0). Please note that the reuse, redistribution and reproduction in particular requires that the authors and source are credited. 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
Holmstrøm, Thomas
Raydan, Daniel
Pedersen, Christian Marcus
Easy access to a carbohydrate-based template for stimuli-responsive surfactants
title Easy access to a carbohydrate-based template for stimuli-responsive surfactants
title_full Easy access to a carbohydrate-based template for stimuli-responsive surfactants
title_fullStr Easy access to a carbohydrate-based template for stimuli-responsive surfactants
title_full_unstemmed Easy access to a carbohydrate-based template for stimuli-responsive surfactants
title_short Easy access to a carbohydrate-based template for stimuli-responsive surfactants
title_sort easy access to a carbohydrate-based template for stimuli-responsive surfactants
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7684687/
https://www.ncbi.nlm.nih.gov/pubmed/33281982
http://dx.doi.org/10.3762/bjoc.16.229
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