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Hydrolase–like catalysis and structural resolution of natural products by a metal–organic framework
The exact chemical structure of non–crystallising natural products is still one of the main challenges in Natural Sciences. Despite tremendous advances in total synthesis, the absolute structural determination of a myriad of natural products with very sensitive chemical functionalities remains undon...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7300120/ https://www.ncbi.nlm.nih.gov/pubmed/32555154 http://dx.doi.org/10.1038/s41467-020-16699-3 |
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author | Mon, Marta Bruno, Rosaria Sanz-Navarro, Sergio Negro, Cristina Ferrando-Soria, Jesús Bartella, Lucia Di Donna, Leonardo Prejanò, Mario Marino, Tiziana Leyva-Pérez, Antonio Armentano, Donatella Pardo, Emilio |
author_facet | Mon, Marta Bruno, Rosaria Sanz-Navarro, Sergio Negro, Cristina Ferrando-Soria, Jesús Bartella, Lucia Di Donna, Leonardo Prejanò, Mario Marino, Tiziana Leyva-Pérez, Antonio Armentano, Donatella Pardo, Emilio |
author_sort | Mon, Marta |
collection | PubMed |
description | The exact chemical structure of non–crystallising natural products is still one of the main challenges in Natural Sciences. Despite tremendous advances in total synthesis, the absolute structural determination of a myriad of natural products with very sensitive chemical functionalities remains undone. Here, we show that a metal–organic framework (MOF) with alcohol–containing arms and adsorbed water, enables selective hydrolysis of glycosyl bonds, supramolecular order with the so–formed chiral fragments and absolute determination of the organic structure by single–crystal X–ray crystallography in a single operation. This combined strategy based on a biomimetic, cheap, robust and multigram available solid catalyst opens the door to determine the absolute configuration of ketal compounds regardless degradation sensitiveness, and also to design extremely–mild metal–free solid–catalysed processes without formal acid protons. |
format | Online Article Text |
id | pubmed-7300120 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-73001202020-06-22 Hydrolase–like catalysis and structural resolution of natural products by a metal–organic framework Mon, Marta Bruno, Rosaria Sanz-Navarro, Sergio Negro, Cristina Ferrando-Soria, Jesús Bartella, Lucia Di Donna, Leonardo Prejanò, Mario Marino, Tiziana Leyva-Pérez, Antonio Armentano, Donatella Pardo, Emilio Nat Commun Article The exact chemical structure of non–crystallising natural products is still one of the main challenges in Natural Sciences. Despite tremendous advances in total synthesis, the absolute structural determination of a myriad of natural products with very sensitive chemical functionalities remains undone. Here, we show that a metal–organic framework (MOF) with alcohol–containing arms and adsorbed water, enables selective hydrolysis of glycosyl bonds, supramolecular order with the so–formed chiral fragments and absolute determination of the organic structure by single–crystal X–ray crystallography in a single operation. This combined strategy based on a biomimetic, cheap, robust and multigram available solid catalyst opens the door to determine the absolute configuration of ketal compounds regardless degradation sensitiveness, and also to design extremely–mild metal–free solid–catalysed processes without formal acid protons. Nature Publishing Group UK 2020-06-17 /pmc/articles/PMC7300120/ /pubmed/32555154 http://dx.doi.org/10.1038/s41467-020-16699-3 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Mon, Marta Bruno, Rosaria Sanz-Navarro, Sergio Negro, Cristina Ferrando-Soria, Jesús Bartella, Lucia Di Donna, Leonardo Prejanò, Mario Marino, Tiziana Leyva-Pérez, Antonio Armentano, Donatella Pardo, Emilio Hydrolase–like catalysis and structural resolution of natural products by a metal–organic framework |
title | Hydrolase–like catalysis and structural resolution of natural products by a metal–organic framework |
title_full | Hydrolase–like catalysis and structural resolution of natural products by a metal–organic framework |
title_fullStr | Hydrolase–like catalysis and structural resolution of natural products by a metal–organic framework |
title_full_unstemmed | Hydrolase–like catalysis and structural resolution of natural products by a metal–organic framework |
title_short | Hydrolase–like catalysis and structural resolution of natural products by a metal–organic framework |
title_sort | hydrolase–like catalysis and structural resolution of natural products by a metal–organic framework |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7300120/ https://www.ncbi.nlm.nih.gov/pubmed/32555154 http://dx.doi.org/10.1038/s41467-020-16699-3 |
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