The synthesis of diphenyl ethers having tyrosine moiety

Tsutomu Inoue, Kenji Naitoh, Seiji Kosemura, Isao Umezawa, Thoru Sonobe, Nobuaki Serizawa, Noboru Mori, Hideji Itokawa

Research output: Contribution to journalArticle

28 Citations (Scopus)

Abstract

Dienone mono-epoxides (13) and (14) were readily reacted with potassium phenoxides to give intermediates (17) and (18) which were subjected to methylation followed by reduction with Zn/AcOH 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 Mar 1
Externally publishedYes

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Phenyl Ethers
Methylation
Epoxy Compounds
Tyrosine
Potassium

ASJC Scopus subject areas

  • Organic Chemistry

Cite this

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

The synthesis of diphenyl ethers having tyrosine moiety. / Inoue, Tsutomu; Naitoh, Kenji; Kosemura, Seiji; Umezawa, Isao; Sonobe, Thoru; Serizawa, Nobuaki; Mori, Noboru; Itokawa, Hideji.

In: Heterocycles, Vol. 20, No. 3, 01.03.1983, p. 397-400.

Research output: Contribution to journalArticle

Inoue, T, Naitoh, K, Kosemura, S, Umezawa, I, Sonobe, T, Serizawa, N, Mori, N & Itokawa, H 1983, 'The synthesis of diphenyl ethers having tyrosine moiety', Heterocycles, vol. 20, no. 3, pp. 397-400.
Inoue T, Naitoh K, Kosemura S, Umezawa I, Sonobe T, Serizawa N et al. The synthesis of diphenyl ethers having tyrosine moiety. Heterocycles. 1983 Mar 1;20(3):397-400.
Inoue, Tsutomu ; Naitoh, Kenji ; Kosemura, Seiji ; Umezawa, Isao ; Sonobe, Thoru ; Serizawa, Nobuaki ; Mori, Noboru ; Itokawa, Hideji. / The synthesis of diphenyl ethers having tyrosine moiety. In: Heterocycles. 1983 ; Vol. 20, No. 3. pp. 397-400.
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