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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...

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Autores principales: Tolnai, Gergely L., Nilsson, Ulf J., Olofsson, Berit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
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.
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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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