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Bis-Cyclometalated Indazole and Benzimidazole Chiral-at-Iridium Complexes: Synthesis and Asymmetric Catalysis

A new class of bis-cyclometalated iridium(III) catalysts containing two inert cyclometalated 6-tert-butyl-2-phenyl-2H-indazole bidentate ligands or two inert cyclometalated 5-tert-butyl-1-methyl-2-phenylbenzimidazoles is introduced. The coordination sphere is complemented by two labile acetonitriles...

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Detalles Bibliográficos
Autores principales: Brunen, Sebastian, Grell, Yvonne, Steinlandt, Philipp S., Harms, Klaus, Meggers, Eric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8037582/
https://www.ncbi.nlm.nih.gov/pubmed/33804954
http://dx.doi.org/10.3390/molecules26071822
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author Brunen, Sebastian
Grell, Yvonne
Steinlandt, Philipp S.
Harms, Klaus
Meggers, Eric
author_facet Brunen, Sebastian
Grell, Yvonne
Steinlandt, Philipp S.
Harms, Klaus
Meggers, Eric
author_sort Brunen, Sebastian
collection PubMed
description A new class of bis-cyclometalated iridium(III) catalysts containing two inert cyclometalated 6-tert-butyl-2-phenyl-2H-indazole bidentate ligands or two inert cyclometalated 5-tert-butyl-1-methyl-2-phenylbenzimidazoles is introduced. The coordination sphere is complemented by two labile acetonitriles, and a hexafluorophosphate ion serves as a counterion for the monocationic complexes. Single enantiomers of the chiral-at-iridium complexes (>99% er) are obtained through a chiral-auxiliary-mediated approach using a monofluorinated salicyloxazoline and are investigated as catalysts in the enantioselective conjugate addition of indole to an α,β-unsaturated 2-acyl imidazole and an asymmetric Nazarov cyclization.
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spelling pubmed-80375822021-04-12 Bis-Cyclometalated Indazole and Benzimidazole Chiral-at-Iridium Complexes: Synthesis and Asymmetric Catalysis Brunen, Sebastian Grell, Yvonne Steinlandt, Philipp S. Harms, Klaus Meggers, Eric Molecules Article A new class of bis-cyclometalated iridium(III) catalysts containing two inert cyclometalated 6-tert-butyl-2-phenyl-2H-indazole bidentate ligands or two inert cyclometalated 5-tert-butyl-1-methyl-2-phenylbenzimidazoles is introduced. The coordination sphere is complemented by two labile acetonitriles, and a hexafluorophosphate ion serves as a counterion for the monocationic complexes. Single enantiomers of the chiral-at-iridium complexes (>99% er) are obtained through a chiral-auxiliary-mediated approach using a monofluorinated salicyloxazoline and are investigated as catalysts in the enantioselective conjugate addition of indole to an α,β-unsaturated 2-acyl imidazole and an asymmetric Nazarov cyclization. MDPI 2021-03-24 /pmc/articles/PMC8037582/ /pubmed/33804954 http://dx.doi.org/10.3390/molecules26071822 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ).
spellingShingle Article
Brunen, Sebastian
Grell, Yvonne
Steinlandt, Philipp S.
Harms, Klaus
Meggers, Eric
Bis-Cyclometalated Indazole and Benzimidazole Chiral-at-Iridium Complexes: Synthesis and Asymmetric Catalysis
title Bis-Cyclometalated Indazole and Benzimidazole Chiral-at-Iridium Complexes: Synthesis and Asymmetric Catalysis
title_full Bis-Cyclometalated Indazole and Benzimidazole Chiral-at-Iridium Complexes: Synthesis and Asymmetric Catalysis
title_fullStr Bis-Cyclometalated Indazole and Benzimidazole Chiral-at-Iridium Complexes: Synthesis and Asymmetric Catalysis
title_full_unstemmed Bis-Cyclometalated Indazole and Benzimidazole Chiral-at-Iridium Complexes: Synthesis and Asymmetric Catalysis
title_short Bis-Cyclometalated Indazole and Benzimidazole Chiral-at-Iridium Complexes: Synthesis and Asymmetric Catalysis
title_sort bis-cyclometalated indazole and benzimidazole chiral-at-iridium complexes: synthesis and asymmetric catalysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8037582/
https://www.ncbi.nlm.nih.gov/pubmed/33804954
http://dx.doi.org/10.3390/molecules26071822
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