| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5219019 | Tetrahedron | 2012 | 5 Pages |
Abstract
This study describes a very efficient strategy for the synthesis of two new bridged-nicotine analogues. Starting from either 4- or 3-chloropyridine the desired tricyclic ring systems are accessed in just three steps in 23% and 40% overall yield, respectively.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
François Crestey, Geert Hooyberghs, Jesper L. Kristensen,