Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5276826 | Tetrahedron Letters | 2007 | 4 Pages |
Abstract
Oxidation of the indolo[2,3-a]carbazole 15, readily obtained in six steps from indigo, followed by deprotection results in formation of the indolo[3,2-j]phenanthridine quinone alkaloid calothrixin B 2, demonstrating the viability of the proposed biosynthetic route to this unique ring system.
Graphical abstractOxidation of the indolo[2,3-a]carbazole 15 results in the biomimetic synthesis of calothrixin B 2.Figure optionsDownload full-size imageDownload as PowerPoint slide
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