Model study for the total synthesis of antifungal australifungin

Construction of α-diketone and β-ketoaldehyde moieties

Kenichi Takao, Seigo Nagata, Susumu Kobayashi, Hisanaka Ito, Takeo Taguchi

Research output: Contribution to journalArticle

3 Citations (Scopus)

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 languageEnglish
Pages (from-to)447-448
Number of pages2
JournalChemistry Letters
Issue number5
Publication statusPublished - 1998
Externally publishedYes

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Aldehydes
Molecules
australifungin

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 journalArticle

Takao, Kenichi ; Nagata, Seigo ; Kobayashi, Susumu ; Ito, Hisanaka ; Taguchi, Takeo. / Model study for the total synthesis of antifungal australifungin : Construction of α-diketone and β-ketoaldehyde moieties. In: Chemistry Letters. 1998 ; No. 5. pp. 447-448.
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