Synthesis and Stereochemical Revision of Violaceoid E, a Polyoxygenated Cyclohexanoid Natural Product Isolated from <i>Aspergillus violaceofuscus</i> Gasperini

The first concise synthesis of the proposed structure of violaceoid E, possessing a cis -diol moiety, has been achieved. However, the spectroscopic data of the synthetic compound were inconsistent with those of the natural product, suggesting that the genuine violaceoid E might be a trans -diol. An efficient synthesis of our proposed trans -diol-type violaceoid E has also been achieved, enabling the establishment of the absolute configuration of natural violaceoid E.

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Publication Details

Journal
Journal of Natural Products
Published
2026-07-01
DOI
https://doi.org/10.1021/acs.jnatprod.6c00630
Primary Topic
Microbial Metabolism and Applications
Type
article
Field-Weighted Citation Impact
0.00
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article

Synthesis and Stereochemical Revision of Violaceoid E, a Polyoxygenated Cyclohexanoid Natural Product Isolated from Aspergillus violaceofuscus Gasperini

Hironori Okamura, Yusuke Ogura, Y Kubo, Hirosato Takikawa
Journal of Natural Products
Microbial Metabolism and Applications
article

Synthesis and Stereochemical Revision of Violaceoid E, a Polyoxygenated Cyclohexanoid Natural Product Isolated from Aspergillus violaceofuscus Gasperini

Hironori Okamura, Yusuke Ogura, Y Kubo, Hirosato Takikawa
article en

Abstract

The first concise synthesis of the proposed structure of violaceoid E, possessing a cis -diol moiety, has been achieved. However, the spectroscopic data of the synthetic compound were inconsistent with those of the natural product, suggesting that the genuine violaceoid E might be a trans -diol. An efficient synthesis of our proposed trans -diol-type violaceoid E has also been achieved, enabling the establishment of the absolute configuration of natural violaceoid E.

Journal of Natural Products
The University of Tokyo (JP)
Openalex Percentile: Top 9%
Microbial Metabolism and Applications
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