Synthesis and antitumor activity of podophyllotoxin aza-analogues
- 1 January 1989
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 30 (22) , 2953-2954
- https://doi.org/10.1016/s0040-4039(00)99167-6
Abstract
No abstract availableThis publication has 13 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 of 2-arylbenzocyclobutenol, a potential intermediate for podophyllotoxin synthesis: Use of lda for benzyne formation and trappingTetrahedron 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