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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...

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Autores principales: Steinlandt, Philipp S., Zuo, Wei, Harms, Klaus, Meggers, Eric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
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).
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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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