Bidirectional, organocatalytic synthesis of lepidopteran sex pheromones
| Autor: | Ting Liu, and David Türp, Jennifer Julis, Raphael Berner, Mathias Christmann, Renata Marcia de Figueiredo |
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| Přispěvatelé: | Institut Charles Gerhardt Montpellier - Institut de Chimie Moléculaire et des Matériaux de Montpellier (ICGM ICMMM), Ecole Nationale Supérieure de Chimie de Montpellier (ENSCM)-Centre National de la Recherche Scientifique (CNRS)-Université de Montpellier (UM)-Université Montpellier 1 (UM1)-Université Montpellier 2 - Sciences et Techniques (UM2)-Institut de Chimie du CNRS (INC), Institute of Inorganic Chemistry [Aachen], Rheinisch-Westfälische Technische Hochschule Aachen (RWTH) |
| Rok vydání: | 2007 |
| Předmět: |
Aldehydes
Magnetic Resonance Spectroscopy Molecular Structure Stereochemistry 010405 organic chemistry Chemistry [CHIM.ORGA]Chemical Sciences/Organic chemistry Organic Chemistry Cameraria ohridella Stereoisomerism General Medicine Ketones 010402 general chemistry Animal origin 01 natural sciences Sensitivity and Specificity Horse chestnut Catalysis 0104 chemical sciences Lepidoptera Evolutionary biology Sex pheromone Animals Sex Attractants |
| Zdroj: | Journal of Organic Chemistry Journal of Organic Chemistry, American Chemical Society, 2006, 72 (2), pp.640-642. ⟨10.1021/jo0620415⟩ |
| ISSN: | 0022-3263 1520-6904 |
| DOI: | 10.1021/jo0620415⟩ |
| Popis: | International audience; 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,10Ztetradeca- 8,10-dienal 5c, from the horse chestnut leafminer (Cameraria ohridella). |
| Databáze: | OpenAIRE |
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