Abstract
Treatment of an α-phenylselenylketone with mercury(II) perchlorate in methanol yielded an α,α-dimethoxyketone; by using this new reaction an erythrinan alkaloid, erysotrine, was synthesized.
| Original language | English |
|---|---|
| Pages (from-to) | 1216-1217 |
| Number of pages | 2 |
| Journal | Journal of the Chemical Society, Chemical Communications |
| Issue number | 18 |
| Publication status | Published - 1984 |
| Externally published | Yes |
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ASJC Scopus subject areas
- Molecular Medicine
Cite this
Application of a new reaction of α-phenylselenylketones to the synthesis of erysotrine. / Tsuda, Yoshisuke; Hosoi, Shinzo; Nakai, Akira; Ohshima, Takeshi; Sakai, Yuki; Kiuchi, Fumiyuki.
In: Journal of the Chemical Society, Chemical Communications, No. 18, 1984, p. 1216-1217.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Application of a new reaction of α-phenylselenylketones to the synthesis of erysotrine
AU - Tsuda, Yoshisuke
AU - Hosoi, Shinzo
AU - Nakai, Akira
AU - Ohshima, Takeshi
AU - Sakai, Yuki
AU - Kiuchi, Fumiyuki
PY - 1984
Y1 - 1984
N2 - Treatment of an α-phenylselenylketone with mercury(II) perchlorate in methanol yielded an α,α-dimethoxyketone; by using this new reaction an erythrinan alkaloid, erysotrine, was synthesized.
AB - Treatment of an α-phenylselenylketone with mercury(II) perchlorate in methanol yielded an α,α-dimethoxyketone; by using this new reaction an erythrinan alkaloid, erysotrine, was synthesized.
UR - http://www.scopus.com/inward/record.url?scp=37049103400&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=37049103400&partnerID=8YFLogxK
M3 - Article
AN - SCOPUS:37049103400
SP - 1216
EP - 1217
JO - Chemical Communications
JF - Chemical Communications
SN - 1359-7345
IS - 18
ER -