Multi-Functionalized 2,2':6',2''-Terpyridines
- Heller, Marcel; Schubert, Ulrich S.
 - Abstract:
 - In this contribution, Stille-type cross-coupling procedure is shown to be an easy and universal way to prepare a variety of functionalized terpyridines. They may be functionalized in one step with different substituents at the outer pyridine rings and at the 4- position of the centered ring, leading to multi-functionalized compounds. The initially obtained methylester and ethylester groups may be simply converted into bromomethyl and hydroxymethyl groups, which allow further functionalization reactions.
 - Year:
 - 2002
 - Type of Publication:
 - Article
 - Keywords:
 - terpyridine synthesis; Stille cross-coupling; functional groups; multidentate ligands; multifunctionality
 - Journal:
 - Synlett
 - Pages:
 - 751 – 754