Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5271862 | Tetrahedron Letters | 2009 | 4 Pages |
Abstract
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.
Graphical abstractObservations 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 full-size imageDownload as PowerPoint slide
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