Multi-functionalized 2,2':6',2''-terpyridines

M. Heller, U.S. Schubert

Onderzoeksoutput: Bijdrage aan tijdschriftTijdschriftartikelAcademicpeer review

26 Citaten (Scopus)
1 Downloads (Pure)


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.
Originele taal-2Engels
Pagina's (van-tot)751-754
Nummer van het tijdschrift5
StatusGepubliceerd - 2002


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