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Evaluation of P-bridged biaryl phosphine ligands in palladium-catalysed Suzuki–Miyaura cross-coupling reactions
A family of biaryl phosphacyclic ligands derived from phobane and phosphatrioxa-adamantane frameworks is described. The rigid biaryl phosphacycles are efficient for Suzuki–Miyaura cross-coupling of aryl bromides and chlorides. In particular, coupling reactions of the challenging sterically hindered...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9037619/ https://www.ncbi.nlm.nih.gov/pubmed/35480011 http://dx.doi.org/10.1039/d1ra04947j |
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author | Lamola, Jairus L. Moshapo, Paseka T. Holzapfel, Cedric W. Maumela, Munaka Christopher |
author_facet | Lamola, Jairus L. Moshapo, Paseka T. Holzapfel, Cedric W. Maumela, Munaka Christopher |
author_sort | Lamola, Jairus L. |
collection | PubMed |
description | A family of biaryl phosphacyclic ligands derived from phobane and phosphatrioxa-adamantane frameworks is described. The rigid biaryl phosphacycles are efficient for Suzuki–Miyaura cross-coupling of aryl bromides and chlorides. In particular, coupling reactions of the challenging sterically hindered and heterocyclic substrates were viable at room temperature. |
format | Online Article Text |
id | pubmed-9037619 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90376192022-04-26 Evaluation of P-bridged biaryl phosphine ligands in palladium-catalysed Suzuki–Miyaura cross-coupling reactions Lamola, Jairus L. Moshapo, Paseka T. Holzapfel, Cedric W. Maumela, Munaka Christopher RSC Adv Chemistry A family of biaryl phosphacyclic ligands derived from phobane and phosphatrioxa-adamantane frameworks is described. The rigid biaryl phosphacycles are efficient for Suzuki–Miyaura cross-coupling of aryl bromides and chlorides. In particular, coupling reactions of the challenging sterically hindered and heterocyclic substrates were viable at room temperature. The Royal Society of Chemistry 2021-08-05 /pmc/articles/PMC9037619/ /pubmed/35480011 http://dx.doi.org/10.1039/d1ra04947j Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Lamola, Jairus L. Moshapo, Paseka T. Holzapfel, Cedric W. Maumela, Munaka Christopher Evaluation of P-bridged biaryl phosphine ligands in palladium-catalysed Suzuki–Miyaura cross-coupling reactions |
title | Evaluation of P-bridged biaryl phosphine ligands in palladium-catalysed Suzuki–Miyaura cross-coupling reactions |
title_full | Evaluation of P-bridged biaryl phosphine ligands in palladium-catalysed Suzuki–Miyaura cross-coupling reactions |
title_fullStr | Evaluation of P-bridged biaryl phosphine ligands in palladium-catalysed Suzuki–Miyaura cross-coupling reactions |
title_full_unstemmed | Evaluation of P-bridged biaryl phosphine ligands in palladium-catalysed Suzuki–Miyaura cross-coupling reactions |
title_short | Evaluation of P-bridged biaryl phosphine ligands in palladium-catalysed Suzuki–Miyaura cross-coupling reactions |
title_sort | evaluation of p-bridged biaryl phosphine ligands in palladium-catalysed suzuki–miyaura cross-coupling reactions |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9037619/ https://www.ncbi.nlm.nih.gov/pubmed/35480011 http://dx.doi.org/10.1039/d1ra04947j |
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