| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5276543 | Tetrahedron Letters | 2007 | 5 Pages |
Abstract
The stereoselective total synthesis of (+)-obtusenyne is described. The oxonene skeleton possessing trans-orientated alkyl substituents at the α,αâ²-positions was stereoselectively constructed via cyclization of the corresponding hydroxy epoxide promoted by Eu(fod)3.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Toshiyuki Uemura, Toshio Suzuki, Naohiro Onodera, Hisahiro Hagiwara, Takashi Hoshi,