ENANTIOSELECTIVE SYNTHESIS OF FLAVONOIDS. PART 2. POLY-OXYGENATED α-HYDROXYDIHYDROCHALCONES AND CIRCULAR DICHROIC ASSESSMENT OF THEIR ABSOLUTE CONFIGURATION

DOI: 10.1016/S0040-4020(01)86778-8

Source and publish data:

Tetrahedron p. 4429 - 4442 (1990)

Update date:2022-08-03

Topics:

Authors:

Augustyn, Jan A. N.

Bezuidenhoudt, Barend C. B.

Swanepoel, Annelie

Ferreira, Daneel

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Article abstract of DOI:10.1016/S0040-4020(01)86778-8

Chiral chalcone epoxides exhibiting the oxygenation patterns of naturally occurring flavonoids and isoflavonoids were transformed into the corresponding α-hydroxydihydrochalcones.The availability of both enantiomers permitted assessment of the absolute co

Full text of DOI:10.1016/S0040-4020(01)86778-8

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