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Attempted synthesis of a meta-metalated calix[4]arene
An evidence for the formation of a rare meta-metalated inherently chiral calix[4]arene is described. Our strategy involved using a mesoionic carbene to direct C–H activation, but proved to form an unexpectedly unstable intermediate that was identified through high-resolution mass spectrometry. On ro...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6719732/ https://www.ncbi.nlm.nih.gov/pubmed/31501666 http://dx.doi.org/10.3762/bjoc.15.195 |
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author | Jurisch, Christopher D Arnott, Gareth E |
author_facet | Jurisch, Christopher D Arnott, Gareth E |
author_sort | Jurisch, Christopher D |
collection | PubMed |
description | An evidence for the formation of a rare meta-metalated inherently chiral calix[4]arene is described. Our strategy involved using a mesoionic carbene to direct C–H activation, but proved to form an unexpectedly unstable intermediate that was identified through high-resolution mass spectrometry. On route to our target, a new optimized method to mononitrocalix[4]arenes was developed, including optimized and high yielding transformations to azide and 1,2,3-triazole derivatives which may have application in other areas of research. |
format | Online Article Text |
id | pubmed-6719732 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-67197322019-09-09 Attempted synthesis of a meta-metalated calix[4]arene Jurisch, Christopher D Arnott, Gareth E Beilstein J Org Chem Full Research Paper An evidence for the formation of a rare meta-metalated inherently chiral calix[4]arene is described. Our strategy involved using a mesoionic carbene to direct C–H activation, but proved to form an unexpectedly unstable intermediate that was identified through high-resolution mass spectrometry. On route to our target, a new optimized method to mononitrocalix[4]arenes was developed, including optimized and high yielding transformations to azide and 1,2,3-triazole derivatives which may have application in other areas of research. Beilstein-Institut 2019-08-22 /pmc/articles/PMC6719732/ /pubmed/31501666 http://dx.doi.org/10.3762/bjoc.15.195 Text en Copyright © 2019, Jurisch and Arnott https://creativecommons.org/licenses/by/4.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0). Please note that the reuse, redistribution and reproduction in particular requires that the authors and source are credited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms) |
spellingShingle | Full Research Paper Jurisch, Christopher D Arnott, Gareth E Attempted synthesis of a meta-metalated calix[4]arene |
title | Attempted synthesis of a meta-metalated calix[4]arene |
title_full | Attempted synthesis of a meta-metalated calix[4]arene |
title_fullStr | Attempted synthesis of a meta-metalated calix[4]arene |
title_full_unstemmed | Attempted synthesis of a meta-metalated calix[4]arene |
title_short | Attempted synthesis of a meta-metalated calix[4]arene |
title_sort | attempted synthesis of a meta-metalated calix[4]arene |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6719732/ https://www.ncbi.nlm.nih.gov/pubmed/31501666 http://dx.doi.org/10.3762/bjoc.15.195 |
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