Design, Synthesis, and Application of a Family of Chiral Non‐C2‐Symmetric NHCs with a Fused Sidechain

Although a considerable number of chiral nitrogen heterocyclic carbenes (NHCs) have been developed yet it is highly necessary to develop new NHCs bearing multiple sites for facile modifications of both electronic nature and steric hindrance. Herein, we uncover a new family of chiral non‐C2‐Symmetric...

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Published inAngewandte Chemie International Edition Vol. 64; no. 27; pp. e202508572 - n/a
Main Authors Cai, Zhen‐Xi, Zhang, Qi, Wei, Tian‐Yu, Tian, Hu, Jiang, Jia‐Wei, Wei, Zhang‐Yi, Yin, Liang
Format Journal Article
LanguageEnglish
Published Weinheim Wiley Subscription Services, Inc 01.07.2025
EditionInternational ed. in English
Subjects
Online AccessGet full text
ISSN1433-7851
1521-3773
1521-3773
DOI10.1002/anie.202508572

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Abstract Although a considerable number of chiral nitrogen heterocyclic carbenes (NHCs) have been developed yet it is highly necessary to develop new NHCs bearing multiple sites for facile modifications of both electronic nature and steric hindrance. Herein, we uncover a new family of chiral non‐C2‐Symmetric NHCs with a fused sidechain, whose precursors are synthesized by a simple five‐step route. The synthesis includes Pd‐catalyzed cross‐coupling or nucleophilic addition/oxidation, chiral phosphoric acid‐catalyzed asymmetric reduction of 2‐aryl‐quinolines, bromination at C8, Buchwald–Hartwig amination, and cyclization with methyl orthoformate. Among nine prepared NHCs, YC‐NHC8 is the optimal ligand for Cu(I)‐catalyzed asymmetric SN2′ silylation, YC‐NHC3 works as the best ligand for Cu(I)‐catalyzed enantioselective conjugate silylation of simple α,β‐unsaturated amides, and YC‐NHC9 serves as the most suitable ligand for copper(I)‐catalyzed asymmetric silylation of azadienes. Remarkably, these three reactions are successfully run under a catalyst loading of 0.1 mol%, indicating that YC‐NHCs may have the potential to be broadly used in efficient asymmetric transition metal catalysis. A new family of chiral non‐C2‐Symmetric NHCs with a fused sidechain was synthesized and used as efficient ligands in three copper(I)‐catalyzed enantioselective reactions at the catalyst loading of 1 mol%, including SN2′ silylation, conjugate silylation of α,β‐unsaturated amides, and silylation of azadienes.
AbstractList Although a considerable number of chiral nitrogen heterocyclic carbenes (NHCs) have been developed, yet it is highly necessary to develop new NHCs bearing multiple sites for facile modifications of both electronic nature and steric hindrance. Herein, we uncover a new family of chiral non-C2-Symmetric NHCs with a fused sidechain, whose precursors are synthesized by a simple five-step route. The synthesis includes Pd-catalyzed cross-coupling or nucleophilic addition/oxidation, chiral phosphoric acid-catalyzed asymmetric reduction of 2-aryl-quinolines, bromination at C8, Buchwald-Hartwig amination, and cyclization with methyl orthoformate. Among nine prepared NHCs, YC-NHC8 is the optimal ligand for Cu(I)-catalyzed asymmetric SN2' silylation, YC-NHC3 works as the best ligand for Cu(I)-catalyzed enantioselective conjugate silylation of simple α,β-unsaturated amides, and YC-NHC9 serves as the most suitable ligand for copper(I)-catalyzed asymmetric silylation of azadienes. Remarkably, these three reactions are successfully run under a catalyst loading of 0.1 mol %, indicating that YC-NHCs may have the potential to be broadly used in efficient asymmetric transition metal catalysis.Although a considerable number of chiral nitrogen heterocyclic carbenes (NHCs) have been developed, yet it is highly necessary to develop new NHCs bearing multiple sites for facile modifications of both electronic nature and steric hindrance. Herein, we uncover a new family of chiral non-C2-Symmetric NHCs with a fused sidechain, whose precursors are synthesized by a simple five-step route. The synthesis includes Pd-catalyzed cross-coupling or nucleophilic addition/oxidation, chiral phosphoric acid-catalyzed asymmetric reduction of 2-aryl-quinolines, bromination at C8, Buchwald-Hartwig amination, and cyclization with methyl orthoformate. Among nine prepared NHCs, YC-NHC8 is the optimal ligand for Cu(I)-catalyzed asymmetric SN2' silylation, YC-NHC3 works as the best ligand for Cu(I)-catalyzed enantioselective conjugate silylation of simple α,β-unsaturated amides, and YC-NHC9 serves as the most suitable ligand for copper(I)-catalyzed asymmetric silylation of azadienes. Remarkably, these three reactions are successfully run under a catalyst loading of 0.1 mol %, indicating that YC-NHCs may have the potential to be broadly used in efficient asymmetric transition metal catalysis.
Although a considerable number of chiral nitrogen heterocyclic carbenes (NHCs) have been developed yet it is highly necessary to develop new NHCs bearing multiple sites for facile modifications of both electronic nature and steric hindrance. Herein, we uncover a new family of chiral non‐C2‐Symmetric NHCs with a fused sidechain, whose precursors are synthesized by a simple five‐step route. The synthesis includes Pd‐catalyzed cross‐coupling or nucleophilic addition/oxidation, chiral phosphoric acid‐catalyzed asymmetric reduction of 2‐aryl‐quinolines, bromination at C8, Buchwald–Hartwig amination, and cyclization with methyl orthoformate. Among nine prepared NHCs, YC‐NHC8 is the optimal ligand for Cu(I)‐catalyzed asymmetric SN2′ silylation, YC‐NHC3 works as the best ligand for Cu(I)‐catalyzed enantioselective conjugate silylation of simple α,β‐unsaturated amides, and YC‐NHC9 serves as the most suitable ligand for copper(I)‐catalyzed asymmetric silylation of azadienes. Remarkably, these three reactions are successfully run under a catalyst loading of 0.1 mol%, indicating that YC‐NHCs may have the potential to be broadly used in efficient asymmetric transition metal catalysis.
Although a considerable number of chiral nitrogen heterocyclic carbenes (NHCs) have been developed yet it is highly necessary to develop new NHCs bearing multiple sites for facile modifications of both electronic nature and steric hindrance. Herein, we uncover a new family of chiral non‐C2‐Symmetric NHCs with a fused sidechain, whose precursors are synthesized by a simple five‐step route. The synthesis includes Pd‐catalyzed cross‐coupling or nucleophilic addition/oxidation, chiral phosphoric acid‐catalyzed asymmetric reduction of 2‐aryl‐quinolines, bromination at C8, Buchwald–Hartwig amination, and cyclization with methyl orthoformate. Among nine prepared NHCs, YC‐NHC8 is the optimal ligand for Cu(I)‐catalyzed asymmetric SN2′ silylation, YC‐NHC3 works as the best ligand for Cu(I)‐catalyzed enantioselective conjugate silylation of simple α,β‐unsaturated amides, and YC‐NHC9 serves as the most suitable ligand for copper(I)‐catalyzed asymmetric silylation of azadienes. Remarkably, these three reactions are successfully run under a catalyst loading of 0.1 mol%, indicating that YC‐NHCs may have the potential to be broadly used in efficient asymmetric transition metal catalysis. A new family of chiral non‐C2‐Symmetric NHCs with a fused sidechain was synthesized and used as efficient ligands in three copper(I)‐catalyzed enantioselective reactions at the catalyst loading of 1 mol%, including SN2′ silylation, conjugate silylation of α,β‐unsaturated amides, and silylation of azadienes.
Author Wei, Tian‐Yu
Zhang, Qi
Yin, Liang
Jiang, Jia‐Wei
Wei, Zhang‐Yi
Tian, Hu
Cai, Zhen‐Xi
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Snippet Although a considerable number of chiral nitrogen heterocyclic carbenes (NHCs) have been developed yet it is highly necessary to develop new NHCs bearing...
Although a considerable number of chiral nitrogen heterocyclic carbenes (NHCs) have been developed, yet it is highly necessary to develop new NHCs bearing...
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SubjectTerms Amides
Amination
Asymmetric catalysis
Asymmetry
Bromination
Catalysis
Chemical synthesis
Chiral NHC
Conjugate silylation
Copper
Copper catalyst
Cross coupling
Enantiomers
Ligands
Organic compounds
Oxidation
Palladium
Phosphoric acid
Quinolines
SN2′ silylation
Steric hindrance
Transition metals
Title Design, Synthesis, and Application of a Family of Chiral Non‐C2‐Symmetric NHCs with a Fused Sidechain
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fanie.202508572
https://www.proquest.com/docview/3229028428
https://www.proquest.com/docview/3193718326
Volume 64
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