A Novel Synthetic Route to 1-Aryltetralin Lignan Lactone Via Intermolecular Cycloaddition with O-qu Inodimethane
- 1 July 1983
- journal article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 13 (9), 787-796
- https://doi.org/10.1080/00397918308063711
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- A convergent mercury mediated lignan synthesisTetrahedron Letters, 1982
- The preparation of lignans via intermolecular cycloadditions with quinodimethanesJournal of the Chemical Society, Chemical Communications, 1982
- A stereocontrolled synthesis of antineoplastic podophyllum lignansJournal of the American Chemical Society, 1981
- An improved route to an intermediate in podophyllotoxin synthesisJournal of the Chemical Society, Chemical Communications, 1980
- Synthesis of Podophyllotoxin1,2The Journal of Organic Chemistry, 1966
- Zur Struktur des Sikkimotoxins I. Synthese von stereoisomeren 6,7‐Dimethoxy‐Analogen des Podophyllotoxins. 11. Mitteilung über mitosehemmende NaturstoffeHelvetica Chimica Acta, 1963
- Compounds Related to Podophyllotoxin. X. Synthesis of Picropodophyllin1Journal of the American Chemical Society, 1960
- The Configuration of the Camphenilyl Amines*Journal of the American Chemical Society, 1951