volume 1991 , issue 11 , pages 1241-1243

Enantioselective synthesis of (S)-(+)-2-tridecanol acetate, an aggregation pheromone component ofDrosophila mulleri

D. Enders ¹

Andrew Plant ¹

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Institut für Organische Chemie der Technischen Hochschule Aachen, Professor‐Pirlet‐Straße 1, W‐5100 Aachen |

Publication type: Journal Article

Publication date: 1991-11-12

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DOI: 10.1002/jlac.1991199101214

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Organic Chemistry

Physical and Theoretical Chemistry

Abstract

The enantioselective synthesis of (S)-(+)-2-tridecanol acetate [(S)-6] (ee = 93.5%), an aggregation pheromone of Drosophila mulleri, is described. Key steps are the α-alkylation of the propiophenone SAMP-hydrazone (S)-2 (de ≥ 96%) and the Baeyer-Villiger reaction of the ketone (S)-4.

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1 citation

Belyaeva Evelina

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PhD in Chemistry

24 publications, 47 citations

h-index: 4

Ufa State Petroleum Technological University

Ufa Federal Research Center of the Russian Academy of Sciences

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