Abstract
Highly oxidated sidechain moiety of antitumor terpentecin and related antibiotics is prepared in a stereoselective manner from diacetone glucose through furanoside intermediates.
| Original language | English |
|---|---|
| Pages (from-to) | 931-932 |
| Number of pages | 2 |
| Journal | Chemistry Letters |
| Issue number | 11 |
| DOIs | |
| Publication status | Published - 1996 Jan 1 |
| Externally published | Yes |
ASJC Scopus subject areas
- Chemistry(all)
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Cite this
Takao, K. I., Aiba, Y., Ito, H., & Kobayashi, S. (1996). Stereoselective route to the highly oxidated sidechain moiety of terpentecin and related antibiotics. Chemistry Letters, (11), 931-932. https://doi.org/10.1246/cl.1996.931