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Homochirality of β‐Peptides: A Significant Biomimetic Property of Unnatural Systems

Homochirality, an interesting phenomenon of life, is mainly an unresolved problem and was thought to be a property of living matter. Herein, we show that artificial β‐peptides have the tendency toward homochiral diastereoselective chain elongation. Chain‐length‐dependent stereochemical discriminatio...

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Autores principales: Mándity, István M., Nekkaa, Imane, Paragi, Gábor, Fülöp, Ferenc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5542748/
https://www.ncbi.nlm.nih.gov/pubmed/28794942
http://dx.doi.org/10.1002/open.201700078
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author Mándity, István M.
Nekkaa, Imane
Paragi, Gábor
Fülöp, Ferenc
author_facet Mándity, István M.
Nekkaa, Imane
Paragi, Gábor
Fülöp, Ferenc
author_sort Mándity, István M.
collection PubMed
description Homochirality, an interesting phenomenon of life, is mainly an unresolved problem and was thought to be a property of living matter. Herein, we show that artificial β‐peptides have the tendency toward homochiral diastereoselective chain elongation. Chain‐length‐dependent stereochemical discrimination was investigated in the synthesis of foldamers with various side chains and secondary structures. It was found that there is a strong tendency toward the synthesis of homochiral oligomers. The size of the side chain drastically influenced the selectivity of the stereodiscriminative chain‐elongation reaction. It is noteworthy that water as the co‐solvent increases the selectivity. Such behavior is a novel fundamental biomimetic property of foldamers with a potential of future industrial application.
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spelling pubmed-55427482017-08-09 Homochirality of β‐Peptides: A Significant Biomimetic Property of Unnatural Systems Mándity, István M. Nekkaa, Imane Paragi, Gábor Fülöp, Ferenc ChemistryOpen Communications Homochirality, an interesting phenomenon of life, is mainly an unresolved problem and was thought to be a property of living matter. Herein, we show that artificial β‐peptides have the tendency toward homochiral diastereoselective chain elongation. Chain‐length‐dependent stereochemical discrimination was investigated in the synthesis of foldamers with various side chains and secondary structures. It was found that there is a strong tendency toward the synthesis of homochiral oligomers. The size of the side chain drastically influenced the selectivity of the stereodiscriminative chain‐elongation reaction. It is noteworthy that water as the co‐solvent increases the selectivity. Such behavior is a novel fundamental biomimetic property of foldamers with a potential of future industrial application. John Wiley and Sons Inc. 2017-07-20 /pmc/articles/PMC5542748/ /pubmed/28794942 http://dx.doi.org/10.1002/open.201700078 Text en © 2017 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Communications
Mándity, István M.
Nekkaa, Imane
Paragi, Gábor
Fülöp, Ferenc
Homochirality of β‐Peptides: A Significant Biomimetic Property of Unnatural Systems
title Homochirality of β‐Peptides: A Significant Biomimetic Property of Unnatural Systems
title_full Homochirality of β‐Peptides: A Significant Biomimetic Property of Unnatural Systems
title_fullStr Homochirality of β‐Peptides: A Significant Biomimetic Property of Unnatural Systems
title_full_unstemmed Homochirality of β‐Peptides: A Significant Biomimetic Property of Unnatural Systems
title_short Homochirality of β‐Peptides: A Significant Biomimetic Property of Unnatural Systems
title_sort homochirality of β‐peptides: a significant biomimetic property of unnatural systems
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5542748/
https://www.ncbi.nlm.nih.gov/pubmed/28794942
http://dx.doi.org/10.1002/open.201700078
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