[Metal–(Nitrogen and/or OxygenPhosphorus‐Based Ligand)]‐Catalyzed Asymmetric Hydrogenation of β‐Amido β‐Substituted Acrylic Esters and Phosphoro Analogs: A Practical Literature Overview

The advent in catalysis of enantiopure (N and/or O)P‐monodentate, bis(N and/or O)P‐, and (N and/or O)P,P‐bidentate ligands is recounted. In particular, their transition‐metal‐complex‐enabled enantioselective CC hydrogenation of archetypal β‐amido β‐(alkyl or aryl)‐vinylcarboxylic esters, phosphonates, and phosphine oxide analogs is reviewed. The efficient P‐ligands are juxtaposed with their reported attained enantioselectivity per substrate alongside the screening conditions. Additional literature pertaining to the asymmetric hydrogenation of the said phosphonates, employing enantiopure diphosphine ligands, is included.

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2026-09-30
DOI
https://doi.org/10.1002/ejoc.70565
Primary Topic
Asymmetric Hydrogenation and Catalysis
Type
article
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article

[Metal–(Nitrogen and/or OxygenPhosphorus‐Based Ligand)]‐Catalyzed Asymmetric Hydrogenation of β‐Amido β‐Substituted Acrylic Esters and Phosphoro Analogs: A Practical Literature Overview

Michel Stephan, Arnald Grabulosa, Barbara Mohar, Marko Jeran
European Journal of Organic Chemistry
Asymmetric Hydrogenation and Catalysis
article

[Metal–(Nitrogen and/or OxygenPhosphorus‐Based Ligand)]‐Catalyzed Asymmetric Hydrogenation of β‐Amido β‐Substituted Acrylic Esters and Phosphoro Analogs: A Practical Literature Overview

Michel Stephan, Arnald Grabulosa, Barbara Mohar, Marko Jeran
article en

Abstract

The advent in catalysis of enantiopure (N and/or O)P‐monodentate, bis(N and/or O)P‐, and (N and/or O)P,P‐bidentate ligands is recounted. In particular, their transition‐metal‐complex‐enabled enantioselective CC hydrogenation of archetypal β‐amido β‐(alkyl or aryl)‐vinylcarboxylic esters, phosphonates, and phosphine oxide analogs is reviewed. The efficient P‐ligands are juxtaposed with their reported attained enantioselectivity per substrate alongside the screening conditions. Additional literature pertaining to the asymmetric hydrogenation of the said phosphonates, employing enantiopure diphosphine ligands, is included.

European Journal of Organic Chemistry
Jožef Stefan Institute (SI), Institut de Nanociència i Nanotecnologia de la Universitat de Barcelona, Universitat de Barcelona (ES)
Openalex Percentile: Top 27%
Asymmetric Hydrogenation and Catalysis
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