Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5279166 | Tetrahedron Letters | 2007 | 4 Pages |
Abstract
An enantioselective approach to the spiroimine fragment of pinnatoxins is described. The strategy is based on a recently developed diastereoselective Ireland-Claisen rearrangement to establish the challenging congested quaternary and tertiary stereocenters within the cyclohexene ring.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Craig E. Stivala, Armen Zakarian,