Circular dichroism spectroscopy as a probe for the stereochemistry of aziridine cleavage reactions of mitomycin C. Application to adducts of mitomycin with DNA constituents
- 1 November 1984
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 106 (24) , 7367-7370
- https://doi.org/10.1021/ja00336a012
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- Studies on the reaction of mitomycin C with potassium ethyl monothiocarbonate under reductive conditionsThe Journal of Organic Chemistry, 1983
- Reactions of mitomycin C with potassium ethyl xanthate in neutral aqueous solutionThe Journal of Organic Chemistry, 1983
- Full structure of a mitomycin C dinucleoside phosphate adduct. Use of differential FT-IR spectroscopy in microscale structural studiesJournal of the American Chemical Society, 1983
- Modification of deoxyribonucleic acid with reductively activated mitomycin C. Structures of modified nucleotides.CHEMICAL & PHARMACEUTICAL BULLETIN, 1983
- 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
- Comparative stereochemistry in the aziridine ring openings of N-methylmitomycin A and 7-methoxy-1,2-(N-methylaziridino)mitoseneJournal of Medicinal Chemistry, 1977
- Chemistry and Structure of Mitomycin C1Journal of Medicinal Chemistry, 1965
- Mitomycins and Porfiromycin: Chemical Mechanism of Activation and Cross-linking of DNAScience, 1964