Furopyridines. XXXI [1]. Birch reduction of furopyridines

Seiji Yamaguchi*, Eriko Hamade, Hajime Yokoyama, Yoshiro Hirai, Shunsaku Shiotani

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

5 Scopus citations

Abstract

Birch reduction of four furopyridines 1a-d effected the characteristic cleavage of the furan ring, giving ethnylpyridinols 2a-d, vinylpyridinols 3b,d, and ethylpyridinols 4a-d, and the reduction of the furan ring, giving dihydrofuropyridine 5c,d.

Original languageEnglish
Pages (from-to)335-339
Number of pages5
JournalJournal of Heterocyclic Chemistry
Volume39
Issue number2
DOIs
StatePublished - 2002

ASJC Scopus subject areas

  • Organic Chemistry
  • Pharmaceutical Science

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