Thermal and palladium catalyzed pericyclic rearrangements of a pentaene ester
- This paper describes thermal and/or palladium promoted pericyclic rearrangements of a pentaene ester. These transformations involve selective double bond isomerizations followed by electrocyclizations, affording a cyclohexadiene and a bicyclic[4.2.0] core resulting from a cyclic triene. © 2004 Elsevier Ltd. All rights reserved.
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