| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5224688 | Tetrahedron | 2009 | 8 Pages |
Abstract
Silacyclic allylsilanes generated through a silene-diene Diels-Alder cycloaddition represent versatile bifunctional reagents for organic synthesis. This is demonstrated in a short stereocontrolled synthesis of (±)-Prelactone B.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Jonathan D. Sellars, Patrick G. Steel,