Anthracene Cycloadducts as Highly Selective Chiral Auxiliaries

Author:

Liu Xiang1,Snyder John K.1

Affiliation:

1. Boston University, Department of Chemistry, Boston, Massachusetts 02215 jsnyder@bu.edu

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

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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