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Isoflavans synthesis

Further illustrations of the value of isoxazole and Heck methodologies in flavone synthesis have been published (95ACS524) and a route to 3-aminoflavone-8-acetic acid has been described (95TL1845). The use of an imidazolidinone chiral auxiliary enables isoflavans to be formed in good yield and in high enantiomeric excess from phenacyl chlorides (95CC1317). [Pg.286]

See other pages where Isoflavans synthesis is mentioned: [Pg.677]    [Pg.677]    [Pg.677]    [Pg.677]    [Pg.677]    [Pg.677]    [Pg.677]    [Pg.677]    [Pg.498]    [Pg.499]    [Pg.498]    [Pg.499]    [Pg.569]    [Pg.240]   


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Isoflavan

Isoflavans

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