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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...

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Autores principales: Gurjar, Kamlesh K., Sharma, Rajendra K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
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.
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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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