| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5277237 | Tetrahedron Letters | 2007 | 4 Pages |
Abstract
In an attempt to synthesize a spiroketal enol ether natural product, we found that treatment of alcohol 5 with Martin's sulfurane did not give the anticipated olefin, but instead afforded ketone 15 through an unprecedented oxidation.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Allison M. Wensley, Andrew O. Hardy, Kay M. Gonsalves, Jennifer L. Koviach,