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Synthetic and computational studies on CuI/ligand pair promoted activation of C(Aryl)-Cl bond in C–N coupling reactions
Cu/ligand-mediated coupling reactions have been widely investigated in the recent past. However, activation of cheaper aryl chlorides is still a great limitation of these reactions. During the course of present investigations efforts have been made to develop a normal and facile CuI/ligand pair prot...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7005438/ https://www.ncbi.nlm.nih.gov/pubmed/32055723 http://dx.doi.org/10.1016/j.heliyon.2020.e03233 |
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author | Gurjar, Kamlesh K. Sharma, Rajendra K. |
author_facet | Gurjar, Kamlesh K. Sharma, Rajendra K. |
author_sort | Gurjar, Kamlesh K. |
collection | PubMed |
description | Cu/ligand-mediated coupling reactions have been widely investigated in the recent past. However, activation of cheaper aryl chlorides is still a great limitation of these reactions. During the course of present investigations efforts have been made to develop a normal and facile CuI/ligand pair protocol for arylation of phthalimide using aryl chlorides. The protocol has also been extended for arylation of amines. On the basis of experimental and theoretical results, a catalytic cycle has also been proposed and it has been established that these reactions follow oxidative addition-reductive elimination (OA-RE) pathway. These studies have indicated that tetracoordinated [Cu(L1)(L2)](+) complex is active catalytic species in these reactions. |
format | Online Article Text |
id | pubmed-7005438 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-70054382020-02-13 Synthetic and computational studies on CuI/ligand pair promoted activation of C(Aryl)-Cl bond in C–N coupling reactions Gurjar, Kamlesh K. Sharma, Rajendra K. Heliyon Article Cu/ligand-mediated coupling reactions have been widely investigated in the recent past. However, activation of cheaper aryl chlorides is still a great limitation of these reactions. During the course of present investigations efforts have been made to develop a normal and facile CuI/ligand pair protocol for arylation of phthalimide using aryl chlorides. The protocol has also been extended for arylation of amines. On the basis of experimental and theoretical results, a catalytic cycle has also been proposed and it has been established that these reactions follow oxidative addition-reductive elimination (OA-RE) pathway. These studies have indicated that tetracoordinated [Cu(L1)(L2)](+) complex is active catalytic species in these reactions. Elsevier 2020-02-04 /pmc/articles/PMC7005438/ /pubmed/32055723 http://dx.doi.org/10.1016/j.heliyon.2020.e03233 Text en © 2020 Published by Elsevier Ltd. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Gurjar, Kamlesh K. Sharma, Rajendra K. Synthetic and computational studies on CuI/ligand pair promoted activation of C(Aryl)-Cl bond in C–N coupling reactions |
title | Synthetic and computational studies on CuI/ligand pair promoted activation of C(Aryl)-Cl bond in C–N coupling reactions |
title_full | Synthetic and computational studies on CuI/ligand pair promoted activation of C(Aryl)-Cl bond in C–N coupling reactions |
title_fullStr | Synthetic and computational studies on CuI/ligand pair promoted activation of C(Aryl)-Cl bond in C–N coupling reactions |
title_full_unstemmed | Synthetic and computational studies on CuI/ligand pair promoted activation of C(Aryl)-Cl bond in C–N coupling reactions |
title_short | Synthetic and computational studies on CuI/ligand pair promoted activation of C(Aryl)-Cl bond in C–N coupling reactions |
title_sort | synthetic and computational studies on cui/ligand pair promoted activation of c(aryl)-cl bond in c–n coupling reactions |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7005438/ https://www.ncbi.nlm.nih.gov/pubmed/32055723 http://dx.doi.org/10.1016/j.heliyon.2020.e03233 |
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