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Peer-reviewedCC BY 4.0Chemistry (Weinheim an Der Bergstrasse, Germany)

Rhodium‐Catalyzed Synthesis of Enantioenriched α‐Substituted Primary Amines Through Asymmetric Transfer Hydrogenation

  1. 1Institute of Chemistry for Life and Health Sciences CNRS, CSB2D Team Paris France
  2. 2Faculty of Pharmaceutical Sciences Shenzhen University of Advanced Technology Shenzhen Guangdong China

Abstract

The preparation of a series of enantioenriched α‐substituted primary amines using rhodium‐catalyzed asymmetric transfer hydrogenation of ortho‐hydroxyaryl N─H imines is reported. The reaction proceeds under mild conditions using a low catalyst loading and ammonium formate as the hydrogen source, delivering the reduced compounds in high yields (up to 99%) and enantioselectivities (up to 99% ee).

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BibTeX
@article{liu2026rhodiumcatalyzed,
  title = {{Rhodium‐Catalyzed Synthesis of Enantioenriched α‐Substituted Primary Amines Through Asymmetric Transfer Hydrogenation}},
  author = {Chonghuo Liu and Guillaume Lefèvre and Qin Yin and Phannarath Phansavath and Virginie Ratovelomanana‐Vidal},
  journal = {Chemistry (Weinheim an Der Bergstrasse, Germany)},
  year = {2026},
  month = jul,
  doi = {10.1002/chem.71466},
  url = {https://doi.org/10.1002/chem.71466},
  note = {CC BY 4.0},
}
RIS
TY  - JOUR
TI  - Rhodium‐Catalyzed Synthesis of Enantioenriched α‐Substituted Primary Amines Through Asymmetric Transfer Hydrogenation
AU  - Chonghuo Liu
AU  - Guillaume Lefèvre
AU  - Qin Yin
AU  - Phannarath Phansavath
AU  - Virginie Ratovelomanana‐Vidal
PY  - 2026
DA  - 2026/07/24
JO  - Chemistry (Weinheim an Der Bergstrasse, Germany)
DO  - 10.1002/chem.71466
UR  - https://doi.org/10.1002/chem.71466
AB  - The preparation of a series of enantioenriched α‐substituted primary amines using rhodium‐catalyzed asymmetric transfer hydrogenation of ortho‐hydroxyaryl N─H imines is reported. The reaction proceeds under mild conditions using a low catalyst loading and ammonium formate as the hydrogen source, delivering the reduced compounds in high yields (up to 99%) and enantioselectivities (up to 99% ee).
SN  - 0947-6539
SN  - 1521-3765
ER  -