| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5279592 | Tetrahedron Letters | 2006 | 4 Pages |
Abstract
The first successful attempt at synthesizing the 11-membered ring of madangamine alkaloids is described. The synthesis involves intramolecular N,O-acetalization of a cyclohexanone derivative, cross-coupling reaction with (Z)-vinylstannane, and intramolecular reductive amination for elaboration of the 11-membered macrocycle.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Yuta Yoshimura, Junji Inoue, Naoki Yamazaki, Sakae Aoyagi, Chihiro Kibayashi,