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Bis‐Cyclometalated Indazole Chiral‐at‐Rhodium Catalyst for Asymmetric Photoredox Cyanoalkylations
A new class of bis‐cyclometalated rhodium(III) catalysts containing two inert cyclometalated 6‐tert‐butyl‐2‐phenyl‐2H‐indazole ligands and two labile acetonitriles is introduced. Single enantiomers (>99 % ee) were obtained through a chiral‐auxiliary‐mediated approach using a monofluorinated salic...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6916287/ https://www.ncbi.nlm.nih.gov/pubmed/31541505 http://dx.doi.org/10.1002/chem.201903369 |
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author | Steinlandt, Philipp S. Zuo, Wei Harms, Klaus Meggers, Eric |
author_facet | Steinlandt, Philipp S. Zuo, Wei Harms, Klaus Meggers, Eric |
author_sort | Steinlandt, Philipp S. |
collection | PubMed |
description | A new class of bis‐cyclometalated rhodium(III) catalysts containing two inert cyclometalated 6‐tert‐butyl‐2‐phenyl‐2H‐indazole ligands and two labile acetonitriles is introduced. Single enantiomers (>99 % ee) were obtained through a chiral‐auxiliary‐mediated approach using a monofluorinated salicyloxazoline. The new chiral‐at‐metal complex is capable of catalyzing the visible‐light‐induced enantioselective α‐cyanoalkylation of 2‐acyl imidazoles in which it serves a dual function as the chiral Lewis acid catalyst for the asymmetric radical chemistry and at the same time as the photoredox catalyst for the visible‐light‐induced redox chemistry (up to 80 % yield, 4:1 d.r., and 95 % ee, 12 examples). |
format | Online Article Text |
id | pubmed-6916287 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-69162872019-12-17 Bis‐Cyclometalated Indazole Chiral‐at‐Rhodium Catalyst for Asymmetric Photoredox Cyanoalkylations Steinlandt, Philipp S. Zuo, Wei Harms, Klaus Meggers, Eric Chemistry Full Papers A new class of bis‐cyclometalated rhodium(III) catalysts containing two inert cyclometalated 6‐tert‐butyl‐2‐phenyl‐2H‐indazole ligands and two labile acetonitriles is introduced. Single enantiomers (>99 % ee) were obtained through a chiral‐auxiliary‐mediated approach using a monofluorinated salicyloxazoline. The new chiral‐at‐metal complex is capable of catalyzing the visible‐light‐induced enantioselective α‐cyanoalkylation of 2‐acyl imidazoles in which it serves a dual function as the chiral Lewis acid catalyst for the asymmetric radical chemistry and at the same time as the photoredox catalyst for the visible‐light‐induced redox chemistry (up to 80 % yield, 4:1 d.r., and 95 % ee, 12 examples). John Wiley and Sons Inc. 2019-11-13 2019-12-02 /pmc/articles/PMC6916287/ /pubmed/31541505 http://dx.doi.org/10.1002/chem.201903369 Text en © 2019 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 Steinlandt, Philipp S. Zuo, Wei Harms, Klaus Meggers, Eric Bis‐Cyclometalated Indazole Chiral‐at‐Rhodium Catalyst for Asymmetric Photoredox Cyanoalkylations |
title | Bis‐Cyclometalated Indazole Chiral‐at‐Rhodium Catalyst for Asymmetric Photoredox Cyanoalkylations |
title_full | Bis‐Cyclometalated Indazole Chiral‐at‐Rhodium Catalyst for Asymmetric Photoredox Cyanoalkylations |
title_fullStr | Bis‐Cyclometalated Indazole Chiral‐at‐Rhodium Catalyst for Asymmetric Photoredox Cyanoalkylations |
title_full_unstemmed | Bis‐Cyclometalated Indazole Chiral‐at‐Rhodium Catalyst for Asymmetric Photoredox Cyanoalkylations |
title_short | Bis‐Cyclometalated Indazole Chiral‐at‐Rhodium Catalyst for Asymmetric Photoredox Cyanoalkylations |
title_sort | bis‐cyclometalated indazole chiral‐at‐rhodium catalyst for asymmetric photoredox cyanoalkylations |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6916287/ https://www.ncbi.nlm.nih.gov/pubmed/31541505 http://dx.doi.org/10.1002/chem.201903369 |
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