Anthracene Cycloadducts as Highly Selective Chiral Auxiliaries
Author:
Affiliation:
1. Boston University, Department of Chemistry, Boston, Massachusetts 02215 jsnyder@bu.edu
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo702724t
Reference17 articles.
1. Recent reviews: (a) Gnas, Y.; Glorius, F.Synthesis2006, 1899. (b) Evans, D. A.; Helmchen, G.; Ruping, M.; Wolfgang, J. InAsymmetric Synthesis: TheEssentials, Christmann, M., Bräse, S., Eds.; Wiley-VCH: Weinheim, Germany, 2007; p 3.
2. Toward the Development of a General Chiral Auxiliary. A Total Synthesis of (+)-Tetronolide via a Tandem Ketene-Trapping [4 + 2] Cycloaddition Strategy
3. Contrasteric carboximide hydrolysis with lithium hydroperoxide
4. Chiral anthracene and anthrone templates as stereocontrolling elements in Diels–Alder/retro Diels–Alder sequences
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