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Efficient O‐Functionalization of Carbohydrates with Electrophilic Reagents
Novel methodology for O‐functionalization of carbohydrate derivatives has been established using bench‐stable and easily prepared iodonium(III) reagents. Both electron‐withdrawing and electron‐donating aryl groups were introduced under ambient conditions and without precautions to exclude air or moi...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5113792/ https://www.ncbi.nlm.nih.gov/pubmed/27528184 http://dx.doi.org/10.1002/anie.201605999 |
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author | Tolnai, Gergely L. Nilsson, Ulf J. Olofsson, Berit |
author_facet | Tolnai, Gergely L. Nilsson, Ulf J. Olofsson, Berit |
author_sort | Tolnai, Gergely L. |
collection | PubMed |
description | Novel methodology for O‐functionalization of carbohydrate derivatives has been established using bench‐stable and easily prepared iodonium(III) reagents. Both electron‐withdrawing and electron‐donating aryl groups were introduced under ambient conditions and without precautions to exclude air or moisture. Furthermore, the approach was extended both to full arylation of cyclodextrin, and to trifluoroethylation of carbohydrate derivatives. This is the first general approach to introduce traditionally non‐electrophilic groups into any of the OH groups around the sugar backbone. The methodology will be useful both in synthetic organic chemistry and biochemistry, as important functional groups can be incorporated under simple and robust reaction conditions in a fast and efficient manner. |
format | Online Article Text |
id | pubmed-5113792 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-51137922016-12-02 Efficient O‐Functionalization of Carbohydrates with Electrophilic Reagents Tolnai, Gergely L. Nilsson, Ulf J. Olofsson, Berit Angew Chem Int Ed Engl Communications Novel methodology for O‐functionalization of carbohydrate derivatives has been established using bench‐stable and easily prepared iodonium(III) reagents. Both electron‐withdrawing and electron‐donating aryl groups were introduced under ambient conditions and without precautions to exclude air or moisture. Furthermore, the approach was extended both to full arylation of cyclodextrin, and to trifluoroethylation of carbohydrate derivatives. This is the first general approach to introduce traditionally non‐electrophilic groups into any of the OH groups around the sugar backbone. The methodology will be useful both in synthetic organic chemistry and biochemistry, as important functional groups can be incorporated under simple and robust reaction conditions in a fast and efficient manner. John Wiley and Sons Inc. 2016-08-16 2016-09-05 /pmc/articles/PMC5113792/ /pubmed/27528184 http://dx.doi.org/10.1002/anie.201605999 Text en © 2016 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Communications Tolnai, Gergely L. Nilsson, Ulf J. Olofsson, Berit Efficient O‐Functionalization of Carbohydrates with Electrophilic Reagents |
title | Efficient O‐Functionalization of Carbohydrates with Electrophilic Reagents |
title_full | Efficient O‐Functionalization of Carbohydrates with Electrophilic Reagents |
title_fullStr | Efficient O‐Functionalization of Carbohydrates with Electrophilic Reagents |
title_full_unstemmed | Efficient O‐Functionalization of Carbohydrates with Electrophilic Reagents |
title_short | Efficient O‐Functionalization of Carbohydrates with Electrophilic Reagents |
title_sort | efficient o‐functionalization of carbohydrates with electrophilic reagents |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5113792/ https://www.ncbi.nlm.nih.gov/pubmed/27528184 http://dx.doi.org/10.1002/anie.201605999 |
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