The oxidation with PCC of atractyligenin 3, the aglicone of the toxic glycoside 1 isolated from Atractylis gummifera L., led to the 15-oxo-derivative 6, together with a small amount of 2,15-dioxoderivative 5, with a selective oxidation of the allylic 15-OH group of the molecule. Further reduction with NaBH4 and KOH hydrolysis gave stereoselectively the 15β-ol epimer of atractiligenin 9.

Camarda L., Ceraulo L., Di Stefano V., Ferrugia M. (1996). Atractyligenin chemistry. Part 4: Synthesis of the 15β-ol epimer of atractyligenin. BOLLETTINO CHIMICO FARMACEUTICO, 135(3), 189-191.

Atractyligenin chemistry. Part 4: Synthesis of the 15β-ol epimer of atractyligenin

Camarda L.
;
Ceraulo L.;Di Stefano V.;Ferrugia M.
1996-01-01

Abstract

The oxidation with PCC of atractyligenin 3, the aglicone of the toxic glycoside 1 isolated from Atractylis gummifera L., led to the 15-oxo-derivative 6, together with a small amount of 2,15-dioxoderivative 5, with a selective oxidation of the allylic 15-OH group of the molecule. Further reduction with NaBH4 and KOH hydrolysis gave stereoselectively the 15β-ol epimer of atractiligenin 9.
Settore CHIM/08 - Chimica Farmaceutica
Settore CHIM/10 - Chimica Degli Alimenti
Camarda L., Ceraulo L., Di Stefano V., Ferrugia M. (1996). Atractyligenin chemistry. Part 4: Synthesis of the 15β-ol epimer of atractyligenin. BOLLETTINO CHIMICO FARMACEUTICO, 135(3), 189-191.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10447/445406
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