Model study for the total synthesis of antifungal australifungin: Construction of α-diketone and β-ketoaldehyde moieties

Ken Ichi Takao; Seigo Nagata; Susumu Kobayashi; Hisanaka Ito; Takeo Taguchi

doi:10.1246/cl.1998.447

Model study for the total synthesis of antifungal australifungin: Construction of α-diketone and β-ketoaldehyde moieties

Ken Ichi Takao, Seigo Nagata, Susumu Kobayashi, Hisanaka Ito, Takeo Taguchi

Department of Applied Chemistry

Research output: Contribution to journal › Article

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 language	English
Pages (from-to)	447-448
Number of pages	2
Journal	Chemistry Letters
Issue number	5
DOIs	https://doi.org/10.1246/cl.1998.447
Publication status	Published - 1998 Jan 1

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ASJC Scopus subject areas

Chemistry(all)

Cite this

Takao, K. I., Nagata, S., Kobayashi, S., Ito, H., & Taguchi, T. (1998). Model study for the total synthesis of antifungal australifungin: Construction of α-diketone and β-ketoaldehyde moieties. Chemistry Letters, (5), 447-448. https://doi.org/10.1246/cl.1998.447

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Access to Document

10.1246/cl.1998.447