Abstract
An oxetane ring can be constructed from 5α-acyloxy-Δ 4(20)-taxoids with osmylation as the first step in the usual manner. The innovation reported here is the use of an intramolecularly available acyl group for the protection of 20-OH by an unexpected 5-to 20-migration under slightly basic conditions.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 99-100 |
| Number of pages | 2 |
| Journal | Chinese Chemical Letters |
| Volume | 8 |
| Issue number | 2 |
| Publication status | Published - 1997 |
| Externally published | Yes |
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ASJC Scopus subject areas
- Chemistry(all)
Cite this
Liu, R., Guo, J. Y., & Liang, X. T. (1997). Construction of the oxetane ring from 5α-acyloxy-Δ 4(20)-taxoids. Chinese Chemical Letters, 8(2), 99-100.