Lignanes. 15. Première Synthèse Totale de la (−)-α-Conidendrine Naturelle
- 1 January 1992
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 48 (4) , 687-694
- https://doi.org/10.1016/s0040-4020(01)88129-1
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- Lignanes, 11. Preparation de la (R)-(+)-β-Vanillyl γ-butyrolactone et Son Utilisation dans la Synthese Totale de Lignanes NaturelsJournal of Natural Products, 1991
- Synthesis of lignans related to the podophyllotoxin seriesJournal of the Chemical Society, Perkin Transactions 1, 1987
- Etudes de lignanesTetrahedron, 1986
- Stereoselective reactions. VIII. Stereochemical requirement for the benzylic oxidation of lignan lactone. A highly selective synthesis of the antitumor lignan lactone steganacin by the oxidation of stegane.CHEMICAL & PHARMACEUTICAL BULLETIN, 1985
- Chemistry of the Podocarpaceae. LXIX. Further Lignans from te Wood of Dacrydium intermediumAustralian Journal of Chemistry, 1985
- Enantioselektive Synthese von (‐)‐(R)‐und(+)‐(S)‐[6]‐Gingerol‐Gewürzprinzip des Ingwers1)European Journal of Inorganic Chemistry, 1979
- Chemistry of the Podocarpaceae. LIV. Lignans from the Wood of Dacrydium intermediumAustralian Journal of Chemistry, 1979