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-Reference-Cited by-同舟云学术

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

Published:2011-07 Issue:13 Volume:22 Page:1448-1454
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Shklyaruck Denis,Matiushenkov Evgenii

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference67 articles.

1. (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

2. Biological activity of (3R,5S,6R)- and (3S,5R,6S)-3,5-dimethyl-6-(methylethyl)-3,4,5,6-tetrahydropyran-2-one, a pheromone ofMacrocentrus grandii (Goidanich) (Hymenoptera: Braconidae)

3. The Structure of the Antibiotic Methymycin1

4. Stoffwechselprodukte von Actinomyceten. 5. Mitteilung. �ber das Lacton der ?-Hydroxy-?, ??, ?-trimethyl-pimelins�ure, ein Abbauprodukt von Narbomycin, Pikromycin und Methymycin

5. Macrolide antibiotic studies. XIII partial absolute configurations of methymycin, neomethymycin, narbomycin and picromycin

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