Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5219792 | Tetrahedron | 2011 | 7 Pages |
Abstract
We herein report a new approach toward the synthesis of uncialamycin, an enediyne natural product isolated from the Streptomyces uncialis, bacteria present on the surface of the lichen Cladonia uncialis. A model for the preparation of uncialamycin has been achieved through a reaction cascade, an acetylide addition to the activated quinoline moiety, and a ring closure reaction as key steps.
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