SYNTHESES TOTALES ET ETUDES DE LIGNANES BIOLOGIQUEMENT ACTIFS. APPLICATION DE L'α-HYDROXYALKYLATION DE β-BENZYL-γ-BUTYROLACTONES A LA CREATION DE SQUELETTES PHENYLTETRALINE ET BISBENZOCYCLOOCTADIENE - 5. SYNTHESE TOTALE DU (+/-)-ATTENUOL

DOI: 10.1016/S0040-4020(01)82448-0

Source and publish data:

Tetrahedron p. 2795 - 2798 (1983)

Update date:2022-07-31

Topics:

Authors:

Loriot, Michel

Brown, Eric

Robin, Jean-Pierre

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Article abstract of DOI:10.1016/S0040-4020(01)82448-0

α-Hydroxyalkylation of β-(3,4-methylenedioxybenzyl)-γ-butyrolactone 5 with p-benzyloxybenzaldehyde, followed by cyclization, reduction of the lactone ring and removal of the benzyl group, afforded the lignan (+/-)-attenuol.

Full text of DOI:10.1016/S0040-4020(01)82448-0

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