The synthesis of diphenyl ethers having tyrosine moiety

Tsutornu Inoue, Kenji Naitoh, Seiji Kosemura, Isaa Umezawa, Thoru Sonobe, Nobuaki Serisawa, Nobaru Mori, Hideji Itokawa

Research output: Contribution to journalArticle

28 Citations (Scopus)

Abstract

Dienone mono-epaxides (13) and (1L) were readily reacted with potassium phenonides to give intermediates (17) and (18) which were subjected to methylation followed by reduction with ZnIAcOH to give the desired diphenyl ethers (15a)-(15f) in good yield.

Original languageEnglish
Pages (from-to)397-400
Number of pages4
JournalHeterocycles
Volume20
Issue number3
Publication statusPublished - 1983 Jan 1
Externally publishedYes

ASJC Scopus subject areas

  • Analytical Chemistry
  • Pharmacology
  • Organic Chemistry

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  • Cite this

    Inoue, T., Naitoh, K., Kosemura, S., Umezawa, I., Sonobe, T., Serisawa, N., Mori, N., & Itokawa, H. (1983). The synthesis of diphenyl ethers having tyrosine moiety. Heterocycles, 20(3), 397-400.