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Absolute Configuration of Small Molecules by Co‐Crystallization

The most reliable method to determine the absolute configuration of chiral molecules is X‐ray crystallography, but small molecules can be difficult to crystallize. We report rapid co‐crystallization of tetraaryladamantanes with small molecules as different as n‐decane to nicotine to produce crystals...

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Detalles Bibliográficos
Autores principales: Krupp, Felix, Frey, Wolfgang, Richert, Clemens
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7540501/
https://www.ncbi.nlm.nih.gov/pubmed/32441841
http://dx.doi.org/10.1002/anie.202004992
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author Krupp, Felix
Frey, Wolfgang
Richert, Clemens
author_facet Krupp, Felix
Frey, Wolfgang
Richert, Clemens
author_sort Krupp, Felix
collection PubMed
description The most reliable method to determine the absolute configuration of chiral molecules is X‐ray crystallography, but small molecules can be difficult to crystallize. We report rapid co‐crystallization of tetraaryladamantanes with small molecules as different as n‐decane to nicotine to produce crystals for X‐ray analysis and the assignment of absolute configuration when the molecules are chiral. A screen of 52 diverse compounds gave inclusion in co‐crystals for 88 % of all cases and a high‐resolution structure in 77 % of cases. Furthermore, starting from three milligrams of analyte, a combination of NMR spectroscopy and X‐ray crystallography produced a full structure in less than three days using an adamantane crystallization chaperone that encapsulates the analyte at room temperature.
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spelling pubmed-75405012020-10-09 Absolute Configuration of Small Molecules by Co‐Crystallization Krupp, Felix Frey, Wolfgang Richert, Clemens Angew Chem Int Ed Engl Communications The most reliable method to determine the absolute configuration of chiral molecules is X‐ray crystallography, but small molecules can be difficult to crystallize. We report rapid co‐crystallization of tetraaryladamantanes with small molecules as different as n‐decane to nicotine to produce crystals for X‐ray analysis and the assignment of absolute configuration when the molecules are chiral. A screen of 52 diverse compounds gave inclusion in co‐crystals for 88 % of all cases and a high‐resolution structure in 77 % of cases. Furthermore, starting from three milligrams of analyte, a combination of NMR spectroscopy and X‐ray crystallography produced a full structure in less than three days using an adamantane crystallization chaperone that encapsulates the analyte at room temperature. John Wiley and Sons Inc. 2020-06-29 2020-09-07 /pmc/articles/PMC7540501/ /pubmed/32441841 http://dx.doi.org/10.1002/anie.202004992 Text en © 2020 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Communications
Krupp, Felix
Frey, Wolfgang
Richert, Clemens
Absolute Configuration of Small Molecules by Co‐Crystallization
title Absolute Configuration of Small Molecules by Co‐Crystallization
title_full Absolute Configuration of Small Molecules by Co‐Crystallization
title_fullStr Absolute Configuration of Small Molecules by Co‐Crystallization
title_full_unstemmed Absolute Configuration of Small Molecules by Co‐Crystallization
title_short Absolute Configuration of Small Molecules by Co‐Crystallization
title_sort absolute configuration of small molecules by co‐crystallization
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7540501/
https://www.ncbi.nlm.nih.gov/pubmed/32441841
http://dx.doi.org/10.1002/anie.202004992
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