| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5273676 | Tetrahedron Letters | 2008 | 4 Pages |
Abstract
The synthesis of the novel benz[c]azocines, 11a and 11b was achieved following an 8-endo-trig selective intramolecular Heck reaction. Optimisation of this reaction demonstrated that inclusion of both tetra-n-butylammonium sulfate and water was essential for its success. No products from the corresponding 7-exo-trig process were encountered under these conditions.
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