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A Se···O bonding catalysis approach to the synthesis of calix[4]pyrroles
Described herein is a chalcogen bonding catalysis approach to the synthesis of calix[4]pyrrole derivatives. The Se···O bonding interactions between selenide catalysts and ketones gave rise to the catalytic activity in the condensation reactions between pyrrole and ketones, leading to the generation...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8941317/ https://www.ncbi.nlm.nih.gov/pubmed/35368584 http://dx.doi.org/10.3762/bjoc.18.36 |
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author | Tong, Qingzhe Zhao, Zhiguo Wang, Yao |
author_facet | Tong, Qingzhe Zhao, Zhiguo Wang, Yao |
author_sort | Tong, Qingzhe |
collection | PubMed |
description | Described herein is a chalcogen bonding catalysis approach to the synthesis of calix[4]pyrrole derivatives. The Se···O bonding interactions between selenide catalysts and ketones gave rise to the catalytic activity in the condensation reactions between pyrrole and ketones, leading to the generation of calix[4]pyrrole derivatives in moderate to high yields. This chalcogen bonding catalysis approach was efficient since only 5 mol % catalyst loading was used to promote the consecutive condensation processes while the reactions could be carried out at room temperature, thus highlighting the potential of this type of nonclassical interactions in catalyzing relative complex transformations. |
format | Online Article Text |
id | pubmed-8941317 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-89413172022-03-31 A Se···O bonding catalysis approach to the synthesis of calix[4]pyrroles Tong, Qingzhe Zhao, Zhiguo Wang, Yao Beilstein J Org Chem Letter Described herein is a chalcogen bonding catalysis approach to the synthesis of calix[4]pyrrole derivatives. The Se···O bonding interactions between selenide catalysts and ketones gave rise to the catalytic activity in the condensation reactions between pyrrole and ketones, leading to the generation of calix[4]pyrrole derivatives in moderate to high yields. This chalcogen bonding catalysis approach was efficient since only 5 mol % catalyst loading was used to promote the consecutive condensation processes while the reactions could be carried out at room temperature, thus highlighting the potential of this type of nonclassical interactions in catalyzing relative complex transformations. Beilstein-Institut 2022-03-18 /pmc/articles/PMC8941317/ /pubmed/35368584 http://dx.doi.org/10.3762/bjoc.18.36 Text en Copyright © 2022, Tong et al. https://creativecommons.org/licenses/by/4.0/This is an open access article licensed under the terms of the Beilstein-Institut Open Access License Agreement (https://www.beilstein-journals.org/bjoc/terms/terms), which is identical to the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) ). The reuse of material under this license requires that the author(s), source and license are credited. Third-party material in this article could be subject to other licenses (typically indicated in the credit line), and in this case, users are required to obtain permission from the license holder to reuse the material. |
spellingShingle | Letter Tong, Qingzhe Zhao, Zhiguo Wang, Yao A Se···O bonding catalysis approach to the synthesis of calix[4]pyrroles |
title | A Se···O bonding catalysis approach to the synthesis of calix[4]pyrroles |
title_full | A Se···O bonding catalysis approach to the synthesis of calix[4]pyrroles |
title_fullStr | A Se···O bonding catalysis approach to the synthesis of calix[4]pyrroles |
title_full_unstemmed | A Se···O bonding catalysis approach to the synthesis of calix[4]pyrroles |
title_short | A Se···O bonding catalysis approach to the synthesis of calix[4]pyrroles |
title_sort | se···o bonding catalysis approach to the synthesis of calix[4]pyrroles |
topic | Letter |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8941317/ https://www.ncbi.nlm.nih.gov/pubmed/35368584 http://dx.doi.org/10.3762/bjoc.18.36 |
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