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Application of N-heterocyclic carbene–Cu(I) complexes as catalysts in organic synthesis: a review

N-Heterocyclic carbenes (NHCs) are a special type of carbenes in which the carbene carbon atom is part of the nitrogen heterocyclic ring. Due to the simplicity of their synthesis and the modularity of their stereoelectronic properties, NHCs have unquestionably emerged as one of the most fascinating...

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Autores principales: Beig, Nosheen, Goyal, Varsha, Bansal, Raj Kumar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10520485/
https://www.ncbi.nlm.nih.gov/pubmed/37767335
http://dx.doi.org/10.3762/bjoc.19.102
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author Beig, Nosheen
Goyal, Varsha
Bansal, Raj Kumar
author_facet Beig, Nosheen
Goyal, Varsha
Bansal, Raj Kumar
author_sort Beig, Nosheen
collection PubMed
description N-Heterocyclic carbenes (NHCs) are a special type of carbenes in which the carbene carbon atom is part of the nitrogen heterocyclic ring. Due to the simplicity of their synthesis and the modularity of their stereoelectronic properties, NHCs have unquestionably emerged as one of the most fascinating and well-known species in chemical science. The remarkable stability of NHCs can be attributed to both kinetic as well as thermodynamic effects caused by its structural features. NHCs constitute a well-established class of new ligands in organometallic chemistry. Although initially NHCs were regarded as pure σ-donor ligands, later experimental and theoretical studies established the presence of a significant back donation from the d-orbital of the metal to the π* orbital of the NHC. Over the last two decades, NHC–metal complexes have been extensively used as efficient catalysts in different types of organic reactions. Of these, NHC–Cu(I) complexes found prominence for various reasons, such as ease of preparation, possibility of structural diversity, low cost, and versatile applications. This article overviews applications of NHC–Cu(I) complexes as catalysts in organic synthesis over the last 12 years, which include hydrosilylation reactions, conjugate addition, [3 + 2] cycloaddition, A(3) reaction, boration and hydroboration, N–H and C(sp(2))–H carboxylation, C(sp(2))–H alkenylation and allylation, C(sp(2))–H arylation, C(sp(2))–H amidation, and C(sp(2))–H thiolation. Preceding the section of applications, a brief description of the structure of NHCs, nature of NHC–metal bond, and methods of preparation of NHC–Cu complexes is provided.
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spelling pubmed-105204852023-09-27 Application of N-heterocyclic carbene–Cu(I) complexes as catalysts in organic synthesis: a review Beig, Nosheen Goyal, Varsha Bansal, Raj Kumar Beilstein J Org Chem Review N-Heterocyclic carbenes (NHCs) are a special type of carbenes in which the carbene carbon atom is part of the nitrogen heterocyclic ring. Due to the simplicity of their synthesis and the modularity of their stereoelectronic properties, NHCs have unquestionably emerged as one of the most fascinating and well-known species in chemical science. The remarkable stability of NHCs can be attributed to both kinetic as well as thermodynamic effects caused by its structural features. NHCs constitute a well-established class of new ligands in organometallic chemistry. Although initially NHCs were regarded as pure σ-donor ligands, later experimental and theoretical studies established the presence of a significant back donation from the d-orbital of the metal to the π* orbital of the NHC. Over the last two decades, NHC–metal complexes have been extensively used as efficient catalysts in different types of organic reactions. Of these, NHC–Cu(I) complexes found prominence for various reasons, such as ease of preparation, possibility of structural diversity, low cost, and versatile applications. This article overviews applications of NHC–Cu(I) complexes as catalysts in organic synthesis over the last 12 years, which include hydrosilylation reactions, conjugate addition, [3 + 2] cycloaddition, A(3) reaction, boration and hydroboration, N–H and C(sp(2))–H carboxylation, C(sp(2))–H alkenylation and allylation, C(sp(2))–H arylation, C(sp(2))–H amidation, and C(sp(2))–H thiolation. Preceding the section of applications, a brief description of the structure of NHCs, nature of NHC–metal bond, and methods of preparation of NHC–Cu complexes is provided. Beilstein-Institut 2023-09-20 /pmc/articles/PMC10520485/ /pubmed/37767335 http://dx.doi.org/10.3762/bjoc.19.102 Text en Copyright © 2023, Beig 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 Review
Beig, Nosheen
Goyal, Varsha
Bansal, Raj Kumar
Application of N-heterocyclic carbene–Cu(I) complexes as catalysts in organic synthesis: a review
title Application of N-heterocyclic carbene–Cu(I) complexes as catalysts in organic synthesis: a review
title_full Application of N-heterocyclic carbene–Cu(I) complexes as catalysts in organic synthesis: a review
title_fullStr Application of N-heterocyclic carbene–Cu(I) complexes as catalysts in organic synthesis: a review
title_full_unstemmed Application of N-heterocyclic carbene–Cu(I) complexes as catalysts in organic synthesis: a review
title_short Application of N-heterocyclic carbene–Cu(I) complexes as catalysts in organic synthesis: a review
title_sort application of n-heterocyclic carbene–cu(i) complexes as catalysts in organic synthesis: a review
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10520485/
https://www.ncbi.nlm.nih.gov/pubmed/37767335
http://dx.doi.org/10.3762/bjoc.19.102
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