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Bench‐Stable N‐Heterocyclic Carbene Nickel Precatalysts for C−C and C−N Bond‐Forming Reactions
Herein, we introduce a new class of bench‐stable N‐heterocyclic carbene (NHC) nickel‐precatalysts for homogeneous nickel‐catalysis. The nickel(II) complexes are readily activated to Ni(0) in situ under mild conditions, via a proposed Heck‐type mechanism. The precatalysts are shown to facilitate carb...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6099443/ https://www.ncbi.nlm.nih.gov/pubmed/30147804 http://dx.doi.org/10.1002/cctc.201800454 |
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author | Strieth‐Kalthoff, Felix Longstreet, Ashley R. Weber, Jessica M. Jamison, Timothy F. |
author_facet | Strieth‐Kalthoff, Felix Longstreet, Ashley R. Weber, Jessica M. Jamison, Timothy F. |
author_sort | Strieth‐Kalthoff, Felix |
collection | PubMed |
description | Herein, we introduce a new class of bench‐stable N‐heterocyclic carbene (NHC) nickel‐precatalysts for homogeneous nickel‐catalysis. The nickel(II) complexes are readily activated to Ni(0) in situ under mild conditions, via a proposed Heck‐type mechanism. The precatalysts are shown to facilitate carbonyl‐ene, hydroalkenylation, and amination reactions. |
format | Online Article Text |
id | pubmed-6099443 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-60994432018-08-24 Bench‐Stable N‐Heterocyclic Carbene Nickel Precatalysts for C−C and C−N Bond‐Forming Reactions Strieth‐Kalthoff, Felix Longstreet, Ashley R. Weber, Jessica M. Jamison, Timothy F. ChemCatChem Full Papers Herein, we introduce a new class of bench‐stable N‐heterocyclic carbene (NHC) nickel‐precatalysts for homogeneous nickel‐catalysis. The nickel(II) complexes are readily activated to Ni(0) in situ under mild conditions, via a proposed Heck‐type mechanism. The precatalysts are shown to facilitate carbonyl‐ene, hydroalkenylation, and amination reactions. John Wiley and Sons Inc. 2018-05-02 2018-07-09 /pmc/articles/PMC6099443/ /pubmed/30147804 http://dx.doi.org/10.1002/cctc.201800454 Text en © 2018 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Full Papers Strieth‐Kalthoff, Felix Longstreet, Ashley R. Weber, Jessica M. Jamison, Timothy F. Bench‐Stable N‐Heterocyclic Carbene Nickel Precatalysts for C−C and C−N Bond‐Forming Reactions |
title | Bench‐Stable N‐Heterocyclic Carbene Nickel Precatalysts for C−C and C−N Bond‐Forming Reactions |
title_full | Bench‐Stable N‐Heterocyclic Carbene Nickel Precatalysts for C−C and C−N Bond‐Forming Reactions |
title_fullStr | Bench‐Stable N‐Heterocyclic Carbene Nickel Precatalysts for C−C and C−N Bond‐Forming Reactions |
title_full_unstemmed | Bench‐Stable N‐Heterocyclic Carbene Nickel Precatalysts for C−C and C−N Bond‐Forming Reactions |
title_short | Bench‐Stable N‐Heterocyclic Carbene Nickel Precatalysts for C−C and C−N Bond‐Forming Reactions |
title_sort | bench‐stable n‐heterocyclic carbene nickel precatalysts for c−c and c−n bond‐forming reactions |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6099443/ https://www.ncbi.nlm.nih.gov/pubmed/30147804 http://dx.doi.org/10.1002/cctc.201800454 |
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