| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5275981 | Tetrahedron Letters | 2007 | 4 Pages |
Abstract
Two cyclopentadienones were generated and both underwent conrotatory electrocyclization as expected based on Woodward–Hoffmann rules. This result lends support to the idea that these ring-closing reactions are, in fact, pericyclic processes.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
