On the synthesis and extraordinary configurational stability of the C9a-hydroxylated mitomycins in the 10-decarbamoyloxy-9-dehydro series. Fully synthetic routes to novel mitomycin congeners
- 1 July 1988
- journal article
- letter
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 53 (14) , 3391-3393
- https://doi.org/10.1021/jo00249a061
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- On the reaction of leucomitosenes with osmium tetraoxide. A route to novel mitomycinsThe Journal of Organic Chemistry, 1988
- A stereospecific route to aziridinomitosanes: the synthesis of novel mitomycin congenersJournal of the American Chemical Society, 1985
- Preparation and biological activities of 10-decarbamoyloxy-9-dehydromitomycin b and its analogs.The Journal of Antibiotics, 1981
- The Total Synthesis of MitomycinsJournal of Natural Products, 1979