A practical strategy to access chiral α-aryloxy carboxylic acids through ion-pairing directed asymmetric hydrogenation

A series of optically active α-aryloxy carboxylic acids were obtained via Chenphos/Rh catalyzed highly efficient asymmetric hydrogenation. The proposed ion-pairing interaction between the ligand and the substrate plays a vital role in achieving high enantioselectivity.

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Veröffentlicht in:Organic Chemistry Frontiers 2020-12, Vol.7 (24), p.4069-4073
Hauptverfasser: Yao, Lin, Ma, Haixia, Nie, Zhuang, Nie, Huifang, Zhang, Dongxu, Wei, Zhao, Shen, Zhanhong, Chen, Weiping, Jiang, Ru, Zhang, Shengyong
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container_issue 24
container_start_page 4069
container_title Organic Chemistry Frontiers
container_volume 7
creator Yao, Lin
Ma, Haixia
Nie, Zhuang
Nie, Huifang
Zhang, Dongxu
Wei, Zhao
Shen, Zhanhong
Chen, Weiping
Jiang, Ru
Zhang, Shengyong
description A series of optically active α-aryloxy carboxylic acids were obtained via Chenphos/Rh catalyzed highly efficient asymmetric hydrogenation. The proposed ion-pairing interaction between the ligand and the substrate plays a vital role in achieving high enantioselectivity.
doi_str_mv 10.1039/D0QO01205J
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source Royal Society Of Chemistry Journals 2008-
subjects Asymmetry
Carboxylic acids
Crystallography
Enantiomers
Hydrogenation
Optical activity
Organic chemistry
Substrates
title A practical strategy to access chiral α-aryloxy carboxylic acids through ion-pairing directed asymmetric hydrogenation
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