Synthesis of Enantiopure 1,2-Diaminobicyclo[2.2.2]octane Derivatives, C1-Symmetric Chiral 1,2-Diamines with a Rigid Bicyclic Backbone
Author:
Affiliation:
1. IBMM, UMR-5247, CNRS, Université Montpellier, ENSCM, Place E. Bataillon, 34095 Montpellier Cedex 5, France
2. CRM2, UMR 7036, CNRS, Université de Lorraine, Boulevard des Aiguillettes, 54506 Vandoeuvre-lès-Nancy, France
Funder
Université de Lorraine
Université de Montpellier
Centre National de la Recherche Scientifique
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.7b00122
Reference58 articles.
1. Medicinal agents incorporating the 1,2-diamine functionality
2. trans-1,2-Diaminocyclohexane Derivatives as Chiral Reagents, Scaffolds, and Ligands for Catalysis: Applications in Asymmetric Synthesis and Molecular Recognition
3. Vicinal Diamino Functionalities as Privileged Structural Elements in Biologically Active Compounds and Exploitation of their Synthetic Chemistry
4. The Chemistry of Vicinal Diamines
5. Nitrogen-Containing Ligands for Asymmetric Homogeneous and Heterogeneous Catalysis
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