Abstract
A model study for the total synthesis of australifungin was performed. Olefinic aldehyde was successfully converted to the target molecule having both α-diketone and β-ketoaldehyde moieties.
| Original language | English |
|---|---|
| Pages (from-to) | 447-448 |
| Number of pages | 2 |
| Journal | Chemistry Letters |
| Issue number | 5 |
| Publication status | Published - 1998 |
| Externally published | Yes |
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ASJC Scopus subject areas
- Chemistry(all)
Cite this
Model study for the total synthesis of antifungal australifungin : Construction of α-diketone and β-ketoaldehyde moieties. / Takao, Kenichi; Nagata, Seigo; Kobayashi, Susumu; Ito, Hisanaka; Taguchi, Takeo.
In: Chemistry Letters, No. 5, 1998, p. 447-448.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Model study for the total synthesis of antifungal australifungin
T2 - Construction of α-diketone and β-ketoaldehyde moieties
AU - Takao, Kenichi
AU - Nagata, Seigo
AU - Kobayashi, Susumu
AU - Ito, Hisanaka
AU - Taguchi, Takeo
PY - 1998
Y1 - 1998
N2 - A model study for the total synthesis of australifungin was performed. Olefinic aldehyde was successfully converted to the target molecule having both α-diketone and β-ketoaldehyde moieties.
AB - A model study for the total synthesis of australifungin was performed. Olefinic aldehyde was successfully converted to the target molecule having both α-diketone and β-ketoaldehyde moieties.
UR - http://www.scopus.com/inward/record.url?scp=0041854542&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0041854542&partnerID=8YFLogxK
M3 - Article
SP - 447
EP - 448
JO - Chemistry Letters
JF - Chemistry Letters
SN - 0366-7022
IS - 5
ER -