Application of silylcupration of alkynes to stereo- and regiospecific formation of trisubstituted alkenes. A short synthesis of yellow scale pheromone-Reference-Cited by-同舟云学术

Application of silylcupration of alkynes to stereo- and regiospecific formation of trisubstituted alkenes. A short synthesis of yellow scale pheromone

Published:1989-01 Issue:37 Volume:30 Page:4913-4914
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Millar Jocelyn G.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference15 articles.

1. Synthesis of (E)-3,9-dimethyl-6-isopropyl-5,8-decadien-1-yl acetate, the sex pheromone of the yellow scale

2. Pheromone synthesis. Stereoselective synthesis of (.+-.)-(E)-6-isopropyl-3,9-dimethyl-5,8-decadienyl acetate, the racemate of the yellow scale pheromone, and its (Z)-isomer.

3. Stereoselective synthesis of (S,E)-6-isopropyl-3,9-dimethyl-5,8-decadienyl acetate, the (S)-enantiomer of the yellow scale pheromone.

4. Synthesis of optically active forms of (E)-6-isopropyl-3,9-dimethyl-5,8-decadienyl acetate, the pheromone of the yellow scale

5. The chemistry of higher order organocuprates

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