Observations in the synthesis of the core of the antitumor illudins via an enyne ring closing metathesis cascade

Observations concerning the synthesis of the core spirocyclic AB-ring system of illudins using an enyne ring closing metathesis (EYRCM) cascade are discussed. Substituent effects, in addition to optimization of the reaction conditions and the olefin tether for the key EYRCM reaction, are examined.

Observations related to the synthesis of the functional spirocyclic AB-ring system found in a variety of illudins via a key enyne ring closing metathesis cascade are described.Figure optionsDownload as PowerPoint slide