The synthesis of diphenyl ethers having tyrosine moiety

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

doi:10.3987/r-1983-03-0397

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 journal › Article › peer-review

29 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 language	English
Pages (from-to)	397-400
Number of pages	4
Journal	Heterocycles
Volume	20
Issue number	3
DOIs	https://doi.org/10.3987/r-1983-03-0397
Publication status	Published - 1983
Externally published	Yes

ASJC Scopus subject areas

Analytical Chemistry
Pharmacology
Organic Chemistry

Access to Document

10.3987/r-1983-03-0397

Cite this

@article{c6b0c91f5e1c4d0f94168241f2b79fb6,

title = "The synthesis of diphenyl ethers having tyrosine moiety",

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.",

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

year = "1983",

doi = "10.3987/r-1983-03-0397",

language = "English",

volume = "20",

pages = "397--400",

journal = "Heterocycles",

issn = "0385-5414",

publisher = "Japan Institute of Heterocyclic Chemistry",

number = "3",

}

TY - JOUR

T1 - The synthesis of diphenyl ethers having tyrosine moiety

AU - Inoue, Tsutornu

AU - Naitoh, Kenji

AU - Kosemura, Seiji

AU - Umezawa, Isaa

AU - Sonobe, Thoru

AU - Serisawa, Nobuaki

AU - Mori, Nobaru

AU - Itokawa, Hideji

PY - 1983

Y1 - 1983

N2 - 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.

AB - 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.

UR - http://www.scopus.com/inward/record.url?scp=0010628281&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0010628281&partnerID=8YFLogxK

U2 - 10.3987/r-1983-03-0397

DO - 10.3987/r-1983-03-0397

M3 - Article

AN - SCOPUS:0010628281

VL - 20

SP - 397

EP - 400

JO - Heterocycles

JF - Heterocycles

SN - 0385-5414

IS - 3

ER -

The synthesis of diphenyl ethers having tyrosine moiety

Abstract

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this