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

M. Heller, U.S. Schubert

Research output: Contribution to journalArticleAcademicpeer-review

24 Citations (Scopus)
1 Downloads (Pure)

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.
Original languageEnglish
Pages (from-to)751-754
JournalSynlett
Issue number5
DOIs
Publication statusPublished - 2002

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