Synthesis, Enantiomer Separation, and Absolute Configuration of 2,6-Oxygenated 9-Azabicyclo[3.3.1]nonanes
Author:
Affiliation:
1. Department of Organic Chemistry, Vilnius University, Naugarduko 24, 03225 Vilnius, Lithuania
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo400506h
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3. Discovery of a New Class of Inhibitors ofMycobacterium tuberculosisProtein Tyrosine Phosphatase B by Biology-Oriented Synthesis
4. Pictet-Spengler Reactions in Aprotic Media. Nb-Benzyl Promoted Retention of Optical Activity in the Synthesis of an Indole Substituted Azabicyclo[3.3.1]nonane, a Key Template for the Synthesis of Macroline Alkaloids
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