| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5274222 | Tetrahedron Letters | 2008 | 4 Pages |
Abstract
The oxepane core of zoapatanol was efficiently synthesized from commercially available 1,2,4-butanetriol, and it was shown to be possible to introduce the angular methyl group at C2′ by the reaction of an intermediate butenolide with diazomethane.
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