Tetrahedron

Enantioselective synthesis of flavonoids. Part 1. Poly-Oxygenated chalcone epoxides

JAN Augustyn, CB Barend, D Ferreira

Index: Augustyn, Jan A. N.; Bezuidenhoudt, Barend C. B.; Ferreira, Daneel Tetrahedron, 1990 , vol. 46, # 7 p. 2651 - 2660

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Citation Number: 48

Abstract

Epoxidation of a series of poly-oxygenated chalcones with H2O2 in the presence of poly-α- aminoacid catalysts afforded chiral aromatic oxygenated epoxides in moderate to high optical yields; their absolute configurations were determined by CD spectroscopy. These chalcone epoxides could, in principle, be used as chirons for enantiomerically enriched dihydroflavonols.

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