Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5227794 | Tetrahedron | 2008 | 7 Pages |
Abstract
A total synthesis of (±)-stemonamide and (±)-isostemonamide has been achieved by using a radical cascade that involves two endo-selective cyclizations. (±)-Stemonamine and (±)-isostemonamine are synthesized by chemoselective reduction of (±)-stemonamide and (±)-isostemonamide, respectively.
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