A Concise Asymmetric Synthesis of Sex Pheromone of Euproctis pseudoconspersa (Strand) and Its Enantiomer

The tea tussock moth, <i>Euproctis pseudoconspersa</i> (Strand), is a serious pest, and its sex pheromone is (<i>R</i>)-10,14-dimethylpentadecyl isobutyrate. A new and concise asymmetric synthesis of the sex pheromone and its enantiomer was accomplished. The chiral methyl of the pheromone was introduced by Evans's template, while the extension of the carbon chain was achieved through Li<sub>2</sub>CuCl<sub>4</sub>-catalyzed coupling of chiral tosylate with Grignard reagent.

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Publication Details

Journal
Molecules
Published
2025-06-06
DOI
https://doi.org/10.3390/molecules30122494
Primary Topic
Insect Pheromone Research and Control
Type
article
Field-Weighted Citation Impact
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article

A Concise Asymmetric Synthesis of Sex Pheromone of Euproctis pseudoconspersa (Strand) and Its Enantiomer

Biyu An, Qinghua Bian, Jiangchun Zhong, Shengli Liu et al.
Molecules
Insect Pheromone Research and Control
article

A Concise Asymmetric Synthesis of Sex Pheromone of Euproctis pseudoconspersa (Strand) and Its Enantiomer

Biyu An, Qinghua Bian, Jiangchun Zhong, Shengli Liu, Dan Liu, Jianan Wang
article en

Abstract

The tea tussock moth, <i>Euproctis pseudoconspersa</i> (Strand), is a serious pest, and its sex pheromone is (<i>R</i>)-10,14-dimethylpentadecyl isobutyrate. A new and concise asymmetric synthesis of the sex pheromone and its enantiomer was accomplished. The chiral methyl of the pheromone was introduced by Evans's template, while the extension of the carbon chain was achieved through Li<sub>2</sub>CuCl<sub>4</sub>-catalyzed coupling of chiral tosylate with Grignard reagent.

MoleculesVol. 30(12)
China Agricultural University (CN)
Openalex Percentile: Top 89%
Insect Pheromone Research and Control
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A Concise Asymmetric Synthesis of Sex Pheromone of Euproctis pseudoconspersa (Strand) and Its Enantiomer — Biyu An, Qinghua Bian, et al. · Molecules (2025) | TGRS Research Map | TGRS