Design, synthesis, and antitumor activity-absolute configuration relationships of podophyllotoxin aza-analogues
- 1 February 1993
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 49 (9) , 1891-1900
- https://doi.org/10.1016/s0040-4020(01)80545-7
Abstract
No abstract availableThis publication has 21 references indexed in Scilit:
- A highly stereoselective synthesis of podophyllotoxin and analogues based on an intramolecular Diels-Alder reactionThe Journal of Organic Chemistry, 1988
- Total synthesis of (±) podophyllotoxinTetrahedron Letters, 1987
- Synthesis of podophyllum lignans via an isolable o-quinonoid pyroneJournal of the Chemical Society, Chemical Communications, 1987
- A direct synthesis ofTetrahedron Letters, 1986
- Total synthesis of (±)-podophyllotoxin and (±)-epipodophyllotoxinTetrahedron, 1986
- Total synthesis of (±) epipodophyllotoxin via a (3 + 2)-cycloaddition strategyTetrahedron Letters, 1986
- Total synthesis of (±)-picropodophylloneJournal of the Chemical Society, Perkin Transactions 1, 1982
- A stereocontrolled synthesis of antineoplastic podophyllum lignansJournal of the American Chemical Society, 1981
- Total synthesis of (.+-.)-4'-demethyl-4-epipodophyllotoxin by insertion-cyclizationThe Journal of Organic Chemistry, 1981
- Synthesis of Podophyllotoxin1,2The Journal of Organic Chemistry, 1966