Synthesis and biological evaluation of novel eunicellin analogues
The intramolecular Diels-Alder reaction of a 2,9-disubstituted hexahydro-Δ 5.6-oxonin derivative 14 afforded two diastereomeric tricyclic eunicellin analogues 15 and 16, which were desilylated to produce the alcohols 17 and 3; these were found to be microtubule stabilising ag...
| Main Authors: | , , , |
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| Format: | Conference item |
| Published: |
2005
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