Cyclopropamitosenes, novel bioreductive anticancer agents. Synthesis of 7-methoxycyclopropamitosene and related indolequinones
- 1 January 1994
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 50 (25) , 7657-7674
- https://doi.org/10.1016/s0040-4020(01)90492-2
Abstract
No abstract availableThis publication has 31 references indexed in Scilit:
- On the origins of the DNA sequence selectivity of mitomycin monoalkylation transformationsJournal of the American Chemical Society, 1992
- Reductively activated mitomycin C: an efficient trapping reagent for electrophilesJournal of the American Chemical Society, 1992
- Sodium dithionite-mediated mitomycin C reductive activation processesTetrahedron Letters, 1992
- Studies on the mechanism of mitomycin C(1) electrophilic transformations: structure-reactivity relationshipsThe Journal of Organic Chemistry, 1992
- Studies on the Chemistry of MitomycinsSynlett, 1992
- Chromium(II) perchlorate: an effective reagent for the preparation of mitomycin C nucleophilic substituted compoundsThe Journal of Organic Chemistry, 1991
- Studies on the use of chromium dichlorate for the reductive activation of Mitomycin CJournal of the American Chemical Society, 1991
- Studies on the bonding specificity for mitomycin C-DNA monoalkylation processesJournal of the American Chemical Society, 1991
- Observations on the activation of mitomycin C. Requirements for C-10 functionalizationJournal of the American Chemical Society, 1990
- Mitomycin analogs I. Indoloquinones as (potential) bisalkylating agentsTetrahedron, 1987