<i>N</i>-Heterocyclic Carbene-Catalyzed Chemo- and Enantioselective Three-Component Esterification/Amidation Relay for Access to Planar Chiral Ferrocene Derivatives

An N-heterocyclic carbene (NHC)-catalyzed three-component esterification/amidation relay strategy was disclosed for facile access to enantio-enriched planar chiral ferrocene derivatives. The esterification and amidation reactions in the catalytic relay proceeded in sequence in both chemoselective and enantioselective fashions. Both experimental and computational methods were used to reveal the reaction mechanism and indicated that both the hydrogen-bonding (H-bonding) interactions and the basic additives in the catalytic system had played crucial roles in the reaction chemo- and stereoselectivities. The planar chiral ferrocene-based ester–amide products showed interesting applications in the synthesis of multiple novel ligands for asymmetric catalysis and the development of chiral bactericides for crop protection.

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Publication Details

Journal
ACS Catalysis
Published
2025-04-01
DOI
https://doi.org/10.1021/acscatal.4c07576
Citations
7
Primary Topic
N-Heterocyclic Carbenes in Organic and Inorganic Chemistry
Type
article
Field-Weighted Citation Impact
6.55

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article

N-Heterocyclic Carbene-Catalyzed Chemo- and Enantioselective Three-Component Esterification/Amidation Relay for Access to Planar Chiral Ferrocene Derivatives

Zhichao Jin, Youlin Deng, Haitao Liu, Yonggui Robin et al.
7 citations
ACS Catalysis
N-Heterocyclic Carbenes in Organic and Inorganic Chemistry
6.55
article

N-Heterocyclic Carbene-Catalyzed Chemo- and Enantioselective Three-Component Esterification/Amidation Relay for Access to Planar Chiral Ferrocene Derivatives

Zhichao Jin, Youlin Deng, Haitao Liu, Yonggui Robin, Donghui Wei, Chaoyang Song, Xinghua Wang, Hui Cai
article en
7 citations

Abstract

An N-heterocyclic carbene (NHC)-catalyzed three-component esterification/amidation relay strategy was disclosed for facile access to enantio-enriched planar chiral ferrocene derivatives. The esterification and amidation reactions in the catalytic relay proceeded in sequence in both chemoselective and enantioselective fashions. Both experimental and computational methods were used to reveal the reaction mechanism and indicated that both the hydrogen-bonding (H-bonding) interactions and the basic additives in the catalytic system had played crucial roles in the reaction chemo- and stereoselectivities. The planar chiral ferrocene-based ester–amide products showed interesting applications in the synthesis of multiple novel ligands for asymmetric catalysis and the development of chiral bactericides for crop protection.

ACS CatalysisVol. 15(8)
Nanyang Technological University (SG), Guizhou University (CN), Zhengzhou University (CN), Shanghai Pesticide Research Institute (CN)
National Research Foundation Singapore, Ministry of Education - Singapore, National Natural Science Foundation of China, Guizhou Science and Technology Department, Higher Education Discipline Innovation Project, National Key Research and Development Program of China
Openalex Percentile: Top 3%
N-Heterocyclic Carbenes in Organic and Inorganic Chemistry
6.55
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<i>N</i>-Heterocyclic Carbene-Catalyzed Chemo- and Enantioselective Three-Component Esterification/Amidation Relay for Access to Planar Chiral Ferrocene Derivatives — Zhichao Jin, Youlin Deng, et al. · ACS Catalysis (2025) | TGRS Research Map | TGRS