1,2-Diamines as the Amine Sources in Amidation and Rhodium-Catalyzed Asymmetric Reductive Amination Cascade Reactions
Author:
Affiliation:
1. College of Chemistry & Pharmacy, Northwest A&F University, Yangling, Shaanxi 712100, China
2. College of Plant Protection, Shaanxi Research Center of Biopesticide Engineering & Technology, Northwest A&F University, Yangling, Shaanxi 712100, China
Funder
China Postdoctoral Science Foundation
Northwest A and F University
National Natural Science Foundation of China
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.2c01728
Reference59 articles.
1. Asymmetric Transfer Hydrogenation of Ketonic Substrates Catalyzed by (η5-C5Me5)MCl Complexes (M = Rh and Ir) of (1S,2S)-N-(p-Toluenesulfonyl)-1,2-diphenylethylenediamine
2. New Chiral Rhodium and Iridium Complexes with Chiral Diamine Ligands for Asymmetric Transfer Hydrogenation of Aromatic Ketones
3. Asymmetric Hydrogenation of Cyclic Imines with an Ionic Cp*Rh(III) Catalyst
4. Metal−Brønsted Acid Cooperative Catalysis for Asymmetric Reductive Amination
5. Asymmetric Transfer Hydrogenation of Imines using Alcohol: Efficiency and Selectivity are Influenced by the Hydrogen Donor
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