Synthesis of viridiofungin A trimethyl ester and determination of the absolute structure of viridiofungin A

Tomoyuki Esumi; Yoshiharu Iwabuchi; Hiroshi Irie; Susumi Hatakeyama

doi:10.1016/S0040-4039(97)10754-7

Synthesis of viridiofungin A trimethyl ester and determination of the absolute structure of viridiofungin A

Tomoyuki Esumi, Yoshiharu Iwabuchi, Hiroshi Irie, Susumi Hatakeyama

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

29 Citations (Scopus)

Abstract

Four diastereoisomeric trimethyl esters of viridiofungin A, a member of novel family of aminoacyl alkyl citrate compounds, were synthesized in a highly stereoselective manner and the absolute configuration of natural viridiofungin A was determined to be 3S,4S,2'S.

Original language	English
Pages (from-to)	877-880
Number of pages	4
Journal	Tetrahedron Letters
Volume	39
Issue number	8
DOIs	https://doi.org/10.1016/S0040-4039(97)10754-7
Publication status	Published - 1998 Feb 19
Externally published	Yes

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/S0040-4039(97)10754-7

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abstract = "Four diastereoisomeric trimethyl esters of viridiofungin A, a member of novel family of aminoacyl alkyl citrate compounds, were synthesized in a highly stereoselective manner and the absolute configuration of natural viridiofungin A was determined to be 3S,4S,2'S.",

author = "Tomoyuki Esumi and Yoshiharu Iwabuchi and Hiroshi Irie and Susumi Hatakeyama",

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T1 - Synthesis of viridiofungin A trimethyl ester and determination of the absolute structure of viridiofungin A

AU - Esumi, Tomoyuki

AU - Iwabuchi, Yoshiharu

AU - Irie, Hiroshi

AU - Hatakeyama, Susumi

PY - 1998/2/19

Y1 - 1998/2/19

N2 - Four diastereoisomeric trimethyl esters of viridiofungin A, a member of novel family of aminoacyl alkyl citrate compounds, were synthesized in a highly stereoselective manner and the absolute configuration of natural viridiofungin A was determined to be 3S,4S,2'S.

AB - Four diastereoisomeric trimethyl esters of viridiofungin A, a member of novel family of aminoacyl alkyl citrate compounds, were synthesized in a highly stereoselective manner and the absolute configuration of natural viridiofungin A was determined to be 3S,4S,2'S.

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U2 - 10.1016/S0040-4039(97)10754-7

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JO - Tetrahedron Letters

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ER -

Synthesis of viridiofungin A trimethyl ester and determination of the absolute structure of viridiofungin A

Abstract

ASJC Scopus subject areas

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