Nitrogen bridgehead compounds. Part X (1). 1H and 13C nmr study of pyrido[1,2‐a]pyrimidines

Gábor Tóth, István Hermecz, Zoltán Mészáros

Research output: Article

31 Citations (Scopus)


By 1H nmr, the predominance of the conformer with a quasi‐axial 6‐methyl group was established for the pyrido[1,2‐a]pyrimidines I‐III. The 13C nmr spectra of I‐III were completely assigned. The conjugative effect of substitution at G‐3 on 1H and 13C chemical shifts of the C‐9 methylene group parallels its effect on reactivity.

Original languageEnglish
Pages (from-to)1181-1184
Number of pages4
JournalJournal of Heterocyclic Chemistry
Issue number6
Publication statusPublished - szept. 1979

ASJC Scopus subject areas

  • Organic Chemistry

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