Hydroalumination of 3-butyn-1-ol: Application to a stereoselective synthesis of (3E,5Z)-3,5-dodecadienyl acetate, the sex pheromone of the leaf roller moth-Reference-Cited by-同舟云学术

Hydroalumination of 3-butyn-1-ol: Application to a stereoselective synthesis of (3E,5Z)-3,5-dodecadienyl acetate, the sex pheromone of the leaf roller moth

Published:1999-12 Issue:50 Volume:55 Page:14243-14250
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Michael Chong J.,Heuft Matthew A.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference23 articles.

1. Identification and synthesis of the sex pheromone of Phtheochroa cranaodes (Lepidoptera: Tortricidae)

2. Synthesis and Characterization of the Four Geometrical Isomers of 3,5-Dodecadienyl Acetate.

3. Attractancy to Male Gypsy Moths 1 of (+)-Disparlures Synthesized by Different Procedures 1

4. Identification of the Female Japanese Beetle Sex Pheromone: Inhibition of Male Response by an Enantiomer

5. Pheromone biology of the tobacco beetle (Lasioderma serricorneF., Anobiidae) with notes on the pheromone antagonism between 4S,6S,7S- and 4S,6S,7R-serricornin

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