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α,β-Enone Borylation by Bis(Pinacolato)Diboron Catalyzed by Cu(3)(BTC)(2) Using Cesium Carbonate as a Base
Cu(3)(BTC)(2) (BTC: 1,3,5-benzenetricarboxylate) as a heterogeneous catalyst in the presence of cesium carbonate as a base is reported for the borylation of α,β-conjugated enones by bis(pinacolato)diboron (B(2)pin(2)). According to the hot-filtration test, Cu(3)(BTC)(2) is acting as a heterogeneous...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8228117/ https://www.ncbi.nlm.nih.gov/pubmed/34070463 http://dx.doi.org/10.3390/nano11061396 |
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author | Dhakshinamoorthy, Amarajothi Alvaro, Mercedes Asiri, Abdullah M. Garcia, Hermenegildo |
author_facet | Dhakshinamoorthy, Amarajothi Alvaro, Mercedes Asiri, Abdullah M. Garcia, Hermenegildo |
author_sort | Dhakshinamoorthy, Amarajothi |
collection | PubMed |
description | Cu(3)(BTC)(2) (BTC: 1,3,5-benzenetricarboxylate) as a heterogeneous catalyst in the presence of cesium carbonate as a base is reported for the borylation of α,β-conjugated enones by bis(pinacolato)diboron (B(2)pin(2)). According to the hot-filtration test, Cu(3)(BTC)(2) is acting as a heterogeneous catalyst. Further, Cu(3)(BTC)(2) exhibits a wide substrate scope and can be reused in consecutive runs, maintaining a crystal structure as evidenced by powder X-ray diffraction (XRD). A suitable mechanism is also proposed for this transformation using Cu(3)(BTC)(2) as catalyst. |
format | Online Article Text |
id | pubmed-8228117 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-82281172021-06-26 α,β-Enone Borylation by Bis(Pinacolato)Diboron Catalyzed by Cu(3)(BTC)(2) Using Cesium Carbonate as a Base Dhakshinamoorthy, Amarajothi Alvaro, Mercedes Asiri, Abdullah M. Garcia, Hermenegildo Nanomaterials (Basel) Communication Cu(3)(BTC)(2) (BTC: 1,3,5-benzenetricarboxylate) as a heterogeneous catalyst in the presence of cesium carbonate as a base is reported for the borylation of α,β-conjugated enones by bis(pinacolato)diboron (B(2)pin(2)). According to the hot-filtration test, Cu(3)(BTC)(2) is acting as a heterogeneous catalyst. Further, Cu(3)(BTC)(2) exhibits a wide substrate scope and can be reused in consecutive runs, maintaining a crystal structure as evidenced by powder X-ray diffraction (XRD). A suitable mechanism is also proposed for this transformation using Cu(3)(BTC)(2) as catalyst. MDPI 2021-05-25 /pmc/articles/PMC8228117/ /pubmed/34070463 http://dx.doi.org/10.3390/nano11061396 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Communication Dhakshinamoorthy, Amarajothi Alvaro, Mercedes Asiri, Abdullah M. Garcia, Hermenegildo α,β-Enone Borylation by Bis(Pinacolato)Diboron Catalyzed by Cu(3)(BTC)(2) Using Cesium Carbonate as a Base |
title | α,β-Enone Borylation by Bis(Pinacolato)Diboron Catalyzed by Cu(3)(BTC)(2) Using Cesium Carbonate as a Base |
title_full | α,β-Enone Borylation by Bis(Pinacolato)Diboron Catalyzed by Cu(3)(BTC)(2) Using Cesium Carbonate as a Base |
title_fullStr | α,β-Enone Borylation by Bis(Pinacolato)Diboron Catalyzed by Cu(3)(BTC)(2) Using Cesium Carbonate as a Base |
title_full_unstemmed | α,β-Enone Borylation by Bis(Pinacolato)Diboron Catalyzed by Cu(3)(BTC)(2) Using Cesium Carbonate as a Base |
title_short | α,β-Enone Borylation by Bis(Pinacolato)Diboron Catalyzed by Cu(3)(BTC)(2) Using Cesium Carbonate as a Base |
title_sort | α,β-enone borylation by bis(pinacolato)diboron catalyzed by cu(3)(btc)(2) using cesium carbonate as a base |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8228117/ https://www.ncbi.nlm.nih.gov/pubmed/34070463 http://dx.doi.org/10.3390/nano11061396 |
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