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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...

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Autores principales: Singh, Abhishek K., Nguyen, Remi, Galy, Nicolas, Haag, Rainer, Sharma, Sunil K., Len, Christophe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
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.
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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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