An enantioselective total synthesis of the stilbenolignan (-)-aiphanol and the determination of its absolute stereochemistry

Banwell, Martin; Chand, Satish; Savage, G Paul

doi:10.1016/j.tetasy.2005.02.035

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An enantioselective total synthesis of the stilbenolignan (-)-aiphanol and the determination of its absolute stereochemistry

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Banwell, Martin; Chand, Satish; Savage, G Paul

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The title natural product (-)-aiphanol has been prepared by total synthesis. A key step involved the asymmetric dihydroxylation of (E)-3,5-dimethoxy-4-(methoxymethoxy)cinnamyl alcohol with the AD-mix-β to give triol (1R,2R)-1-(3′,5′-dimethoxy-4′-me

Collections	ANU Research Publications
Date published:	2005
Type:	Journal article
URI:	http://hdl.handle.net/1885/76045
Source:	Tetrahedron: Asymmetry
DOI:	10.1016/j.tetasy.2005.02.035

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An enantioselective total synthesis of the stilbenolignan (-)-aiphanol and the determination of its absolute stereochemistry

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