Synthesis of Multiply Arylated Pyridines
- Papers published
- Asako, T.; Hayashi, W.; Suzuki, S.; Amaike, K.; Itami, K.; Muto, K.; Yamaguchi, J., Tetrahedron 2017, accepted (Invited contribution). DOI: 10.1016/j.tet.2017.03.095
- We have achieved a synthesis of multiply arylated pyridines by using a [4+2] cycloaddition of 2,4-diaryl-5-chloroxazoles and cinnamic acids as a key reaction. The resulting hydroxytriarylpyridines can be derivatized into triarylpyridines, tetraarylpyridines and pentaarylpyridines by sequential cross-couplings. This synthetic method allows for facile and rapid access to highly arylated pyridines with different aryl substituents.