| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5278010 | Tetrahedron Letters | 2008 | 4 Pages |
Abstract
A new, short and efficient route to louisianins C and D is described in which the pyridine ring is constructed from a disubstituted 1,2,4-triazine by an inverse-electron-demand Diels-Alder/retro-Diels-Alder/aromatisation cascade sequence. This eight-step route produces louisianin C in 16% overall yield from the commercially available 5-chloropent-1-yne.
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Authors
Nicola Catozzi, Pierre Wasnaire, Richard J.K. Taylor,