Abstract
A short synthesis of the epoxide fragment of the azinomycins is described. The desired (2S,3S)-stereochemistry was established using an asymmetric dihydroxylation reaction.
| Original language | English |
|---|---|
| Pages (from-to) | 973 |
| Number of pages | 3 |
| Journal | Synlett |
| Issue number | 10 |
| Publication status | Published - Oct 1996 |
Keywords
- azinomycins
- asymmetric dihydroxylation
- STEREOSELECTIVE SYNTHESIS
- ANTITUMOR ANTIBIOTICS
- CONVENIENT SYNTHESIS
- CARZINOPHILIN
- FRAGMENT
- STEREOCHEMISTRY
- CYTOTOXICITY
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