Synthesis of 5-<i>epi</i>- and 10-<i>epi</i>-β-selinenes and 5-<i>epi</i>- and 10-<i>epi</i>-costals and their acaricidal activity against <i>Varroa destructor</i>

Synthesis of 5-epi- and 10-epi-β-selinenes and 5-epi- and 10-epi-costals was achieved from dihydrocarvone, involving the radical cyclization of selenoester to construct a decalone framework as the key step. The acaricidal activities of these diastereomers of (+)-costal and (+)-β-selinene were also evaluated against Varroa destructor. Among them, 10-epi-costal exhibited the most potent acaricidal activity.

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Publication Details

Journal
Bioscience Biotechnology and Biochemistry
Published
2025-03-17
DOI
https://doi.org/10.1093/bbb/zbaf034
Citations
1
Primary Topic
Insect and Pesticide Research
Type
article
Field-Weighted Citation Impact
1.67
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article

Synthesis of 5-epi- and 10-epi-β-selinenes and 5-epi- and 10-epi-costals and their acaricidal activity against Varroa destructor

Yusuke Ogura, Kento Miura, Hirosato Takikawa, Kenji Nemoto
1 citations
Bioscience Biotechnology and Biochemistry
Insect and Pesticide Research
1.67
article

Synthesis of 5-epi- and 10-epi-β-selinenes and 5-epi- and 10-epi-costals and their acaricidal activity against Varroa destructor

Yusuke Ogura, Kento Miura, Hirosato Takikawa, Kenji Nemoto
article en
1 citations

Abstract

Synthesis of 5-epi- and 10-epi-β-selinenes and 5-epi- and 10-epi-costals was achieved from dihydrocarvone, involving the radical cyclization of selenoester to construct a decalone framework as the key step. The acaricidal activities of these diastereomers of (+)-costal and (+)-β-selinene were also evaluated against Varroa destructor. Among them, 10-epi-costal exhibited the most potent acaricidal activity.

Bioscience Biotechnology and BiochemistryVol. 89(6)
Tokyo University of Pharmacy and Life Sciences (JP), The University of Tokyo (JP)
Openalex Percentile: Top 21%
Insect and Pesticide Research
1.67
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