Polycyclic N-Heterocyclic Compounds. 48. Syntheses of Furo[2,3-h]-[1,6]naphthyridine and Imidazo(or Pyrimido)[2,1-f]-[1,6]naphthyridines with Rearrangement

Kenji Sasaki, Abu Shara Shamsur Rouf, Takashi Hirota

Research output: Contribution to journalArticle

19 Citations (Scopus)

Abstract

The formation of a novel ring system, furo[2,3-h][1,6]naphthyridine via the Smiles rearrangement and intramolecular cyclization is described. Cyclization of 5-(ω-hydroxyalky Iamino)-8-methyl-1,2-dihydrofuro[2,3-h][1,6]naphthyridines provided novel spiro compound with rearrangement.

Original languageEnglish
Pages (from-to)49-52
Number of pages4
JournalJournal of Heterocyclic Chemistry
Volume33
Issue number1
Publication statusPublished - 1996

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Naphthyridines
Heterocyclic Compounds
Cyclization
Spiro Compounds

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  • Organic Chemistry

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Polycyclic N-Heterocyclic Compounds. 48. Syntheses of Furo[2,3-h]-[1,6]naphthyridine and Imidazo(or Pyrimido)[2,1-f]-[1,6]naphthyridines with Rearrangement. / Sasaki, Kenji; Rouf, Abu Shara Shamsur; Hirota, Takashi.

In: Journal of Heterocyclic Chemistry, Vol. 33, No. 1, 1996, p. 49-52.

Research output: Contribution to journalArticle

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