Bidirectional, organocatalytic synthesis of lepidopteran sex pheromones

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Abstract

Shuffling of two simple building blocks and a regioselective transfer hydrogenation allow for the rapid synthesis of a small collection of lepidopteran sex pheromones, e.g., 8E,10Z-tetradeca-8,10-dienal 5c, from the horse chestnut leafminer (Cameraria ohridella). © 2007 American Chemical Society.

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De Figueiredo, R. M., Berner, R., Julis, J., Liu, T., Türp, D., & Christmann, M. (2007). Bidirectional, organocatalytic synthesis of lepidopteran sex pheromones. Journal of Organic Chemistry, 72(2), 640–642. https://doi.org/10.1021/jo0620415

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