Asymmetric Transfer Hydrogenation of α-Keto Amides; Highly Enantioselective Formation of Malic Acid Diamides and α-Hydroxyamides
Author:
Affiliation:
1. Department of Chemistry, The University of Warwick, Coventry CV4 7AL, U.K.
Funder
Royal Society
Science and Engineering Research Board
European Regional Development Fund
Advantage West Midlands
University of Warwick
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.1c02830
Reference51 articles.
1. The Golden Age of Transfer Hydrogenation
2. The Development of Phosphine-Free "Tethered" Ruthenium(II) Catalysts for the Asymmetric Reduction of Ketones and Imines
3. Escaping from Flatland: Stereoconvergent Synthesis of Three‐Dimensional Scaffolds via Ruthenium(II)‐Catalyzed Noyori–Ikariya Transfer Hydrogenation
4. Ru‐TsDPEN catalysts and derivatives in asymmetric transfer hydrogenation reactions
5. Recent Developments in Asymmetric Hydrogenation and Transfer Hydrogenation of Ketones and Imines through Dynamic Kinetic Resolution
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