Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5276171 | Tetrahedron Letters | 2007 | 4 Pages |
Abstract
A highly stereoselective total synthesis of arenastatin A, an extremely potent cytotoxic cyclic depsipeptide from marine sponge, was developed. The desired 7,8-β-epoxide in arenastatin A was constructed by asymmetric sulfur ylide-mediated epoxidation in good yield and highly stereoselective manner.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Naoyuki Kotoku, Fuminori Narumi, Tomoya Kato, Miho Yamaguchi, Motomasa Kobayashi,