| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5269900 | Tetrahedron Letters | 2010 | 4 Pages |
Abstract
The total synthesis of lactonamycin has been achieved. The synthesis includes sequential intramolecular conjugate addition of alcohols to the acetylenic ester, stereoselective glycosylation of the tertiary alcohol, and Michael-Dieckmann type cyclization with the thioester, by which the highly convergent route has been established.
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Authors
Kuniaki Tatsuta, Hiroaki Tanaka, Hitomi Tsukagoshi, Takafumi Kashima, Seijiro Hosokawa,