Synthesis of (1R,3S,5S)-1,3,8-Trimethyl-2,9-dioxabicyclo[3.3.1]non-7-ene, the Male Pheromone of a Hepialid MothEndoclita excrescens, and Its Enantiomer-Reference-Cited by-同舟云学术

Synthesis of (1R,3S,5S)-1,3,8-Trimethyl-2,9-dioxabicyclo[3.3.1]non-7-ene, the Male Pheromone of a Hepialid MothEndoclita excrescens, and Its Enantiomer

Published:2002-01 Issue:1 Volume:31 Page:40-41
ISSN:0366-7022
Container-title:Chemistry Letters
language:en
Short-container-title:Chem. Lett.

Author:

Marukawa Kaoru,Mori Kenji

Publisher

The Chemical Society of Japan

Subject

General Chemistry

Reference6 articles.

1. A facile construction of the 2,9-dioxabicyclo-[3.3.1]- non-7-en-6-one ring system: A model for tirandanycin.

2. Total synthesis of the (+)-pheromone of the male swift moth L.

3. Synthesis of both the enantiomers of the heterocyclic pheromones isolated from the male swift moth l

4. Enantioselective synthesis of haminol-1, an alarm pheromone of a mediterranean mollusc

5. Lanthanoids in organic synthesis. 6. Reduction of .alpha.-enones by sodium borohydride in the presence of lanthanoid chlorides: synthetic and mechanistic aspects

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1. ChemInform Abstract: Synthesis of (1R,3S,5S)-1,3,8-Trimethyl-2,9-dioxabicyclo[3.3.1]non-7-ene, the Male Pheromone of a Hepialid Moth Endoclita excrescens, and Its Enantiomer.;ChemInform;2010-05-21

2. Pheromones of Terrestrial Invertebrates;Comprehensive Natural Products II;2010

3. Synthesis of Pheromones: Highlights from 2002-2004;Current Organic Chemistry;2009-03-01

4. Synthesis of (1R,3S,5S)-1,3,8-Trimethyl-2,9-dioxabicyclo[3.3.1]non-7-ene, the Male Pheromone of a Hepialid Moth, Endoclita excrescens, and Its Enantiomer;European Journal of Organic Chemistry;2002-12