A New, Short, and Stereocontrolled Synthesis of C2-Symmetric 1,2-Diamines
Author:
Affiliation:
1. Department of Chemistry and Chemical Biology, Harvard University, Cambridge, Massachusetts 02138, United States
Funder
Pfizer
Bristol-Myers Squibb
Gilead Sciences
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.7b01768
Reference39 articles.
1. The Chemistry of Vicinal Diamines
2. bCorey, E. J.; Kurti, L.Enantioselective Chemical Synthesis;Direct Books Publishing and Elsevier, 2010; pp18–23, 41-2.
3. New enantioselective routes to biologically interesting compounds
4. Stereospecific Synthesis of C2 Symmetric Diamines from the Mother Diamine by Resonance-Assisted Hydrogen-Bond Directed Diaza-Cope Rearrangement
5. Stereospecific Synthesis of Alkyl-Substituted Vicinal Diamines from the Mother Diamine: Overcoming the “Intrinsic Barrier” to the Diaza-Cope Rearrangement Reaction
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