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Englerin A Synthesis

Posted by naturalproductman on October 30, 2009

Mathias Christmann and co-workers at TU Dortmund University in Germany have reported on the total synthesis of englerin A – a sesquiterpene with highly attractive bioactivity. The seven membered ring was accessed via a ring closing metathesis reaction.

englerin A

ACIEE paper

This entry was posted on October 30, 2009 at 9:18 am and is filed under Methodology, Sesquiterpenes, Seven-Membered Rings, Transition Metal. You can follow any responses to this entry through the RSS 2.0 feed. You can leave a response, or trackback from your own site.

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