Asymmetric Synthesis of Axially Chiral N, N‐1,2‐Pentatomic Heterobiaryl Diamines by an Organocatalytic Arylation Reaction

The utilization of axially chiral biaryl diamines has been widely acknowledged as highly advantageous structures for the advancement of chiral catalysts and ligands. This highlights their extensive range of applications in asymmetric catalysis and synthesis. Herein, we devised a direct arylation reactions of 5-aminopyrazoles with azonaphthalenes, utilizing chiral phosphoric acid as the catalyst. This method delivers structurally novel atroposelective N, N-1,2-azole heteroaryl diamines with high yields (up to >98 %) and good to excellent enantiomeric ratios while exhibiting a wide range of substrate compatibility.

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Publication Details

Journal
Chemistry - A European Journal
Published
2024-09-21
DOI
https://doi.org/10.1002/chem.202402843
Citations
7
Primary Topic
Axial and Atropisomeric Chirality Synthesis
Type
article
Field-Weighted Citation Impact
1.75
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article

Asymmetric Synthesis of Axially Chiral N, N‐1,2‐Pentatomic Heterobiaryl Diamines by an Organocatalytic Arylation Reaction

Xiu‐Xiu Qiao, Ganpeng Li, Yonghui He, Qian Li et al.
7 citations
Chemistry - A European Journal
Axial and Atropisomeric Chirality Synthesis
1.75
article

Asymmetric Synthesis of Axially Chiral N, N‐1,2‐Pentatomic Heterobiaryl Diamines by an Organocatalytic Arylation Reaction

Xiu‐Xiu Qiao, Ganpeng Li, Yonghui He, Qian Li, Shi‐Na Zhao, Xiaojing Zhao
article en
7 citations

Abstract

The utilization of axially chiral biaryl diamines has been widely acknowledged as highly advantageous structures for the advancement of chiral catalysts and ligands. This highlights their extensive range of applications in asymmetric catalysis and synthesis. Herein, we devised a direct arylation reactions of 5-aminopyrazoles with azonaphthalenes, utilizing chiral phosphoric acid as the catalyst. This method delivers structurally novel atroposelective N, N-1,2-azole heteroaryl diamines with high yields (up to >98 %) and good to excellent enantiomeric ratios while exhibiting a wide range of substrate compatibility.

Chemistry - A European JournalVol. 30(70)
Minzu University of China (CN), State Ethnic Affairs Commission (CN)
Openalex Percentile: Top 16%
Axial and Atropisomeric Chirality Synthesis
1.75
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Asymmetric Synthesis of Axially Chiral N, N‐1,2‐Pentatomic Heterobiaryl Diamines by an Organocatalytic Arylation Reaction — Xiu‐Xiu Qiao, Ganpeng Li, et al. · Chemistry - A European Journal (2024) | TGRS Research Map | TGRS