| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5266440 | Tetrahedron Letters | 2013 | 5 Pages |
Abstract
Herein, we demonstrate the versatility of the pipecolic linker for the structural diversification of secondary amines with potential CNS activity. The solid-phase methods elaborated involved N1-indole sulfonylation, nitroindole and nitroarene reduction, and microwave-assisted Buchwald-Hartwig N-arylation.
Related Topics
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Authors
PaweÅ Zajdel, Nicolas Masurier, Vittorio Canale, Pascal Verdie, Muriel Amblard, Maciej PawÅowski, Jean Martinez, Gilles Subra,