A diastereoselective synthesis of (1SR,3SR,7RS)-3-methyl-α-himachalene, the sex pheromone of the sandfly, Lutzomyia longipalpis (Diptera: Psychodidae)-Reference-Cited by-同舟云学术

A diastereoselective synthesis of (1SR,3SR,7RS)-3-methyl-α-himachalene, the sex pheromone of the sandfly, Lutzomyia longipalpis (Diptera: Psychodidae)

Published:2012-06 Issue:25 Volume:68 Page:5102-5108
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Dufour Samuel,Castets Pascalie,Pickett John A.,Hooper Antony M.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference14 articles.

1. Epidemiology and ecology of leishmaniasis in Latin-America

2. Chemical analysis of the abdominal glands of two forms ofLutzomyia longipalpis:site of a possible sex pheromone?

3. 9-Methylgermacrene-B is confirmed as the sex pheromone of the sandfly Lutzomyia longipalpis from Lapinha, Brazil, and the absolute stereochemistry defined as S

4. 3-Methyl-α-himachalene is confirmed, and the relative stereochemistry defined, by synthesis as the sex pheromone of the sandfly Lutzomyia longipalpis from Jacobina, Brazil

5. Synthesis of Germacrene-B and Its Extension to the Synthesis of (±)-9-Methylgermacrene-B, the Racemate of the Male-Produced Sex Pheromone of the SandflyLutzomyia longipalpis from Lapinha, Brazil

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