Asymmetric synthesis XXIV : benzoquinolizidine analogues of podophyllotixin via the CN(R, S) method.
- 1 November 1991
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 32 (22) , 2489-2492
- https://doi.org/10.1016/s0040-4039(00)74362-0
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Asymmetric synthesis. 21. The first enantioselective synthesis of natural (+)-tetraponerine-8: a new extension of the CN(R,S) method to an uncommon skeletonThe Journal of Organic Chemistry, 1990
- Synthesis of 2-azapodophyllotoxinTetrahedron Letters, 1989
- The synthesis of 2-azapodophyllotoxinsTetrahedron Letters, 1989
- The synthesis of 4-desoxy-2-azapodophyllotoxinsTetrahedron Letters, 1989
- Synthesis and antitumor activity of podophyllotoxin aza-analoguesTetrahedron Letters, 1989
- Synthesis of etoposide lactam via a mitsunobu reaction sequenceTetrahedron Letters, 1989
- Methylenedioxy-benzopyran analogs of podophyllotoxin, a new synthetic class of antimitotic agents that inhibit tubulin polymerizationBiochemical Pharmacology, 1988
- In vivo antitumor activity of 6-benzyl-1,3-benzodioxole derivatives against the P388, L1210, B16, and M5076 murine modelsJournal of Medicinal Chemistry, 1987
- Chiral 1,4-dihydropyridine equivalents: a new approach to the asymmetric synthesis of alkaloids. The enantiospecific synthesis of (+)- and (-)-coniine and dihydropinidineJournal of the American Chemical Society, 1983
- Studies on the Anti-tumor Activity of Isoquinoline Derivatives. : III. On the Relationship between Toxicity and Chemical Constitution of Isoquinoline DerivativesYAKUGAKU ZASSHI, 1968