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

Research output: Contribution to journal › Article › peer-review

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
Externally published	Yes

ASJC Scopus subject areas

Chemistry(all)

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10.1246/cl.1998.447

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

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.",

author = "Takao, {Ken Ichi} and Seigo Nagata and Susumu Kobayashi and Hisanaka Ito and Takeo Taguchi",

year = "1998",

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AU - Takao, Ken Ichi

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AU - Kobayashi, Susumu

AU - Ito, Hisanaka

AU - Taguchi, Takeo

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

Abstract

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