Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5278969 | Tetrahedron Letters | 2007 | 5 Pages |
Abstract
A simple protocol for the efficient preparation of substituted 6-phenyl-2,2′-bipyridine derivatives is described. An inverse Diels–Alder reaction between a 3-phenyl-5-pyridyl-1,2,4-triazine and an electron-rich ethynyl species at high temperature provides a mixture of two products easily separable by column chromatography. The most encumbered isomer is favoured, likely due to favourable π–π stacking interactions in the transition state. A variety of those ligands suitable for the synthesis of cyclo-metallated complexes have been produced.
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