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 language | English |
|---|---|
| Pages (from-to) | 397-400 |
| Number of pages | 4 |
| Journal | Heterocycles |
| Volume | 20 |
| Issue number | 3 |
| Publication status | Published - 1983 Mar 1 |
| Externally published | Yes |
Fingerprint
ASJC Scopus subject areas
- Organic Chemistry
Cite this
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 journal › Article
}
TY - JOUR
T1 - The synthesis of diphenyl ethers having tyrosine moiety
AU - Inoue, Tsutomu
AU - Naitoh, Kenji
AU - Kosemura, Seiji
AU - Umezawa, Isao
AU - Sonobe, Thoru
AU - Serizawa, Nobuaki
AU - Mori, Noboru
AU - Itokawa, Hideji
PY - 1983/3/1
Y1 - 1983/3/1
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=0010628281&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0010628281&partnerID=8YFLogxK
M3 - Article
AN - SCOPUS:0010628281
VL - 20
SP - 397
EP - 400
JO - Heterocycles
JF - Heterocycles
SN - 0385-5414
IS - 3
ER -