Asymmetric synthesis of a sex pheromone (3S,5R,6S)-3,5-dimethyl-6-isopropyl-3,4,5,6-tetrahydropyran-2-one
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis
Reference18 articles.
1. Chemical Stimuli in Host-Seeking Behavior of Macrocentrus grandii (Hymenoptera: Braconidae)
2. Insect Parasitoids: Finding New Opportunities for Biological Control
3. Contemporary frontiers in insect semiochemical research
4. (3R*,5S*,6R*)-3,5-dimethyl-6-(methylethyl)-3,4,5,6-tetrahydropyran-2-one, a third sex pheromone component forMacrocentrus grandii (goidanich) (Hymenoptera: Braconidae) and evidence for its utility at eclosion
5. Prelog-Djerassi Lactonic Acid. A Target for Design and Development of Stereoselective Synthetic Methods
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1. Addition To C=O Bonds II;Key Chiral Auxiliary Applications;2014
2. Asymmetric Synthesis of Simplactones A and B;Helvetica Chimica Acta;2011-08
3. Stereoselective synthesis of (3S,5S,6S)-tetrahydro-6-isopropyl-3,5-dimethylpyran-2-one; a C5-epimer of a component of a natural sex pheromone of the wasp Macrocentrus grandii, the larval parasitoid of the European corn borer Ostrinia nubilalis;Tetrahedron: Asymmetry;2011-07
4. Five-Membered Ring Systems;Progress in Heterocyclic Chemistry;2011
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