[3,3]Sigmatropic ring expansion of cyclic thionocarbonates. 5. Stereoselective synthesis of the yellow scale pheromone
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference11 articles.
1. Stereoselective synthesis of (S,E)-6-isopropyl-3,9-dimethyl-5,8-decadienyl acetate, the (S)-enantiomer of the yellow scale pheromone.
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. Synthesis of optically active forms of (E)-6-isopropyl-3,9-dimethyl-5,8-decadienyl acetate, the pheromone of the yellow scale
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5. Copper Chloride-Catalyzed and Hydrochloric Acid-Mediated Chemoselective Protiodestannylations of Alkyl (Z)- or (E)-2,3-Bis(trimethylstannyl)-2-alkenoates. Stereoselective Preparation of Alkyl (E)- and (Z)-3-Trimethylstannyl-2-alkenoates;The Journal of Organic Chemistry;1997-08-01
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