Synthesis of virtually enantiopure aminodiols with three adjacent stereogenic centers by epoxidation and ring-opening
Author:
Affiliation:
1. Department of Chemistry
2. The University of Chicago
3. Chicago
4. USA
5. Molecular Catalyst Research Center
Abstract
Synthesis of virtually enantiopure aminodiols with three consecutive stereocenters is accomplished by a sequential cascade of epoxidation and ring-opening.
Funder
National Institutes of Health
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2015/OB/C5OB01808K
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