Synthesis of new phenylpyridyl scaffolds using the Garlanding approach |
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Authors: | Anne Sophie Voisin-Chiret,Gré gory Burzicki,Filomena Corbo,Carlo Franchini |
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Affiliation: | a University of Caen Basse-Normandie, U.F.R. des Sciences Pharmaceutiques, Centre d’Etudes et de Recherche sur le Médicament de Normandie, UPRES EA-4258, FR CNRS INC3M, boulevard Becquerel, 14032 Caen Cedex, France b University of Bari, Department of Pharmaceutical Chemistry, Via E. Orabona n.4, 70125 Bari, Italy |
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Abstract: | One-pot reaction for the synthesis of novel phenylpyridyl derivatives and mixed quater phenylpyridyl compounds is described by using the Garlanding approach. The reactions proceed with moderate to good yields in mild conditions and good reaction times. This work represents a second application of the simplicity and versatility of Garlanding concept for the construction of new phenylpyridyl scaffolds, which can be considered as non-peptidic foldamer α-helix mimetics. |
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Keywords: | Boron Cross-coupling Palladium Pyridines Regioselectivity |
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