Ring-Opening and -Expansion of 2,2′-Biaziridine: Access to Diverse Enantiopure Linear and Bicyclic Vicinal Diamines
Author:
Affiliation:
1. School of Chemistry, University of Wollongong, Wollongong, NSW 2522, Australia
2. Research School of Chemistry, The Australian National University, Canberra, ACT 0200, Australia
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol502164b
Reference62 articles.
1. The Chemistry of Vicinal Diamines
2. Vicinal Diamino Functionalities as Privileged Structural Elements in Biologically Active Compounds and Exploitation of their Synthetic Chemistry
3. Chiral Tertiary Diamines in Asymmetric Synthesis
4. Asymmetric Synthesis of Diverse Glycolic Acid Scaffolds via Dynamic Kinetic Resolution of α-Keto Esters
5. Controlling helical chirality of cobalt complexes by chirality transfer from vicinal diamines
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