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Chemo-Enzymatic Synthesis of Oligoglycerol Derivatives
A cleaner and greener method has been developed and used to synthesize 14 different functionalized oligomer derivatives of glycerol in moderate 29%–39% yields over three steps. After successive regioselective enzymatic acylation of the primary hydroxyl groups, etherification or esterification of the...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273276/ https://www.ncbi.nlm.nih.gov/pubmed/27517886 http://dx.doi.org/10.3390/molecules21081038 |
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author | Singh, Abhishek K. Nguyen, Remi Galy, Nicolas Haag, Rainer Sharma, Sunil K. Len, Christophe |
author_facet | Singh, Abhishek K. Nguyen, Remi Galy, Nicolas Haag, Rainer Sharma, Sunil K. Len, Christophe |
author_sort | Singh, Abhishek K. |
collection | PubMed |
description | A cleaner and greener method has been developed and used to synthesize 14 different functionalized oligomer derivatives of glycerol in moderate 29%–39% yields over three steps. After successive regioselective enzymatic acylation of the primary hydroxyl groups, etherification or esterification of the secondary hydroxyl groups and chemoselective enzymatic saponification, the target compounds can efficiently be used as versatile building blocks in organic and supramolecular chemistry. |
format | Online Article Text |
id | pubmed-6273276 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62732762018-12-28 Chemo-Enzymatic Synthesis of Oligoglycerol Derivatives Singh, Abhishek K. Nguyen, Remi Galy, Nicolas Haag, Rainer Sharma, Sunil K. Len, Christophe Molecules Article A cleaner and greener method has been developed and used to synthesize 14 different functionalized oligomer derivatives of glycerol in moderate 29%–39% yields over three steps. After successive regioselective enzymatic acylation of the primary hydroxyl groups, etherification or esterification of the secondary hydroxyl groups and chemoselective enzymatic saponification, the target compounds can efficiently be used as versatile building blocks in organic and supramolecular chemistry. MDPI 2016-08-09 /pmc/articles/PMC6273276/ /pubmed/27517886 http://dx.doi.org/10.3390/molecules21081038 Text en © 2016 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Singh, Abhishek K. Nguyen, Remi Galy, Nicolas Haag, Rainer Sharma, Sunil K. Len, Christophe Chemo-Enzymatic Synthesis of Oligoglycerol Derivatives |
title | Chemo-Enzymatic Synthesis of Oligoglycerol Derivatives |
title_full | Chemo-Enzymatic Synthesis of Oligoglycerol Derivatives |
title_fullStr | Chemo-Enzymatic Synthesis of Oligoglycerol Derivatives |
title_full_unstemmed | Chemo-Enzymatic Synthesis of Oligoglycerol Derivatives |
title_short | Chemo-Enzymatic Synthesis of Oligoglycerol Derivatives |
title_sort | chemo-enzymatic synthesis of oligoglycerol derivatives |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6273276/ https://www.ncbi.nlm.nih.gov/pubmed/27517886 http://dx.doi.org/10.3390/molecules21081038 |
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