Taxane diterpenes .3. Formation of the eight-membered B-ring by semi-pinacol rearrangement
The substituted furan carboxaldehyde 15 was converted into enone 20 via a stereoselective intramolecular pyrylium ylide-alkene cyclization. Subsequent elaboration of 20 into the triflate 23, followed by solvolysis in acidic trifluoroethanol resulted in quantitative rearrangement to the taxane B/C co...
| Main Authors: | , , , , , , |
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| Formato: | Journal article |
| Idioma: | English |
| Publicado em: |
1996
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