Syntheses and reactivity of trans-6-azabicyclo[3.1.0]hexan-2-ol derivatives and indanol[1,2-b]aziridine. Structural analogs of mitomycin C
- 1 August 1983
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 48 (17) , 2857-2866
- https://doi.org/10.1021/jo00165a015
Abstract
No abstract availableThis publication has 12 references indexed in Scilit:
- Reductive metabolism and alkylating activity of mitomycin C induced by rat liver microsomesBiochemistry, 1981
- Alkylation reactions of mitomycin C at acid pHJournal of the American Chemical Society, 1979
- Studies related to antitumor antibiotics. Part XIV. Reactions of mitomycin B with DNACanadian Journal of Biochemistry, 1978
- Bioactivation as a Model for Drug Design Bioreductive AlkylationScience, 1977
- Comparative stereochemistry in the aziridine ring openings of N-methylmitomycin A and 7-methoxy-1,2-(N-methylaziridino)mitoseneJournal of Medicinal Chemistry, 1977
- Studies on the mode of action of the mitomycin antibiotics. Reversible conversion of mitomycin C into sodium 7-aminomitosane-9a-sulfonateJournal of the American Chemical Society, 1976
- Studies related to antitumor antibiotics. Part V. Reactions of mitomycin C with DNA examined by ethidium fluorescence assayCanadian Journal of Biochemistry, 1976
- The Site of Alkylation of Nucleic Acids by Mitomycin*Biochemistry, 1965
- Chemistry and Structure of Mitomycin C1Journal of Medicinal Chemistry, 1965
- Mitomycins and Porfiromycin: Chemical Mechanism of Activation and Cross-linking of DNAScience, 1964