Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Tong, Qingzhe, Zhao, Zhiguo, Wang, Yao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2022
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
_version_ 1784673085281009664
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
work_keys_str_mv AT tongqingzhe aseobondingcatalysisapproachtothesynthesisofcalix4pyrroles
AT zhaozhiguo aseobondingcatalysisapproachtothesynthesisofcalix4pyrroles
AT wangyao aseobondingcatalysisapproachtothesynthesisofcalix4pyrroles
AT tongqingzhe seobondingcatalysisapproachtothesynthesisofcalix4pyrroles
AT zhaozhiguo seobondingcatalysisapproachtothesynthesisofcalix4pyrroles
AT wangyao seobondingcatalysisapproachtothesynthesisofcalix4pyrroles