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Synthesis and Electrophysiological Testing of Carbonyl Pheromone Analogues for Carposinid Moths

[Image: see text] Sex pheromone analogues were synthesized and tested on two pest carposinid moth species: the guava moth, Coscinoptycha improbana, and the raspberry bud moth, Heterocrossa rubophaga. The pheromone analogues used for the electroantennogram testing included (Z)-11-methylenenonadec-7-e...

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Autores principales: Twidle, Andrew M., Pilkington, Lisa I., Suckling, David M., Barker, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8375095/
https://www.ncbi.nlm.nih.gov/pubmed/34423209
http://dx.doi.org/10.1021/acsomega.1c02614
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author Twidle, Andrew M.
Pilkington, Lisa I.
Suckling, David M.
Barker, David
author_facet Twidle, Andrew M.
Pilkington, Lisa I.
Suckling, David M.
Barker, David
author_sort Twidle, Andrew M.
collection PubMed
description [Image: see text] Sex pheromone analogues were synthesized and tested on two pest carposinid moth species: the guava moth, Coscinoptycha improbana, and the raspberry bud moth, Heterocrossa rubophaga. The pheromone analogues used for the electroantennogram testing included (Z)-11-methylenenonadec-7-ene, (Z)-nonadec-12-en-9-amine, (Z)-11-methoxynonadec-7-ene, (Z)-1-(octylsulfinyl)-dec-3-ene, and (Z)-nonadec-12-en-9-ol. An imine analogue, N-((Z)-nonadec-12-en-9-ylidene)cyclopropanamine, was also synthesized but was too unstable for testing with the moths. None of the analogue compounds elicited significant responses from the male moth antennae.
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spelling pubmed-83750952021-08-20 Synthesis and Electrophysiological Testing of Carbonyl Pheromone Analogues for Carposinid Moths Twidle, Andrew M. Pilkington, Lisa I. Suckling, David M. Barker, David ACS Omega [Image: see text] Sex pheromone analogues were synthesized and tested on two pest carposinid moth species: the guava moth, Coscinoptycha improbana, and the raspberry bud moth, Heterocrossa rubophaga. The pheromone analogues used for the electroantennogram testing included (Z)-11-methylenenonadec-7-ene, (Z)-nonadec-12-en-9-amine, (Z)-11-methoxynonadec-7-ene, (Z)-1-(octylsulfinyl)-dec-3-ene, and (Z)-nonadec-12-en-9-ol. An imine analogue, N-((Z)-nonadec-12-en-9-ylidene)cyclopropanamine, was also synthesized but was too unstable for testing with the moths. None of the analogue compounds elicited significant responses from the male moth antennae. American Chemical Society 2021-08-05 /pmc/articles/PMC8375095/ /pubmed/34423209 http://dx.doi.org/10.1021/acsomega.1c02614 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Twidle, Andrew M.
Pilkington, Lisa I.
Suckling, David M.
Barker, David
Synthesis and Electrophysiological Testing of Carbonyl Pheromone Analogues for Carposinid Moths
title Synthesis and Electrophysiological Testing of Carbonyl Pheromone Analogues for Carposinid Moths
title_full Synthesis and Electrophysiological Testing of Carbonyl Pheromone Analogues for Carposinid Moths
title_fullStr Synthesis and Electrophysiological Testing of Carbonyl Pheromone Analogues for Carposinid Moths
title_full_unstemmed Synthesis and Electrophysiological Testing of Carbonyl Pheromone Analogues for Carposinid Moths
title_short Synthesis and Electrophysiological Testing of Carbonyl Pheromone Analogues for Carposinid Moths
title_sort synthesis and electrophysiological testing of carbonyl pheromone analogues for carposinid moths
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8375095/
https://www.ncbi.nlm.nih.gov/pubmed/34423209
http://dx.doi.org/10.1021/acsomega.1c02614
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