Construction of the Decalin Moiety of Pyrroindomycins

Natural products in the pyrroindomycin family have attracted considerable interest because of their antimicrobial activity, complex structures, and biosynthetic route. However, parts of their structures remain incompletely determined, and there are no reports of a total synthesis to date. In this study, we report on construction of the trans ‐decalin moiety of pyrroindomycins. This knowledge will aid in the determination of the full structure and experimental reproduction of the biosynthesis.

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2026-03-31
DOI
https://doi.org/10.1002/ejoc.70450
Primary Topic
Microbial Natural Products and Biosynthesis
Type
article
Field-Weighted Citation Impact
0.00

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article

Construction of the Decalin Moiety of Pyrroindomycins

Jun Ishihara, Hayato Fukuda, Keita Komine, Tomohiro Tsutsumi
European Journal of Organic Chemistry
Microbial Natural Products and Biosynthesis
article

Construction of the Decalin Moiety of Pyrroindomycins

Jun Ishihara, Hayato Fukuda, Keita Komine, Tomohiro Tsutsumi
article en

Abstract

Natural products in the pyrroindomycin family have attracted considerable interest because of their antimicrobial activity, complex structures, and biosynthetic route. However, parts of their structures remain incompletely determined, and there are no reports of a total synthesis to date. In this study, we report on construction of the trans ‐decalin moiety of pyrroindomycins. This knowledge will aid in the determination of the full structure and experimental reproduction of the biosynthesis.

European Journal of Organic ChemistryVol. 29(16)
Nagasaki University (JP)
Japan Society for the Promotion of Science
Openalex Percentile: Top 33%
Microbial Natural Products and Biosynthesis
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