A highly stereo- and regioselective synthesis of (E)-1,3-dienes and (E,E)-1,3,5-trienes was written by Hayashi, Toshio;Yanagida, Masako;Matsuda, Yuko;Oishi, Takeshi. And the article was included in Tetrahedron Letters in 1983.Recommanded Product: (E)-Dodeca-9,11-dien-1-yl acetate The following contents are mentioned in the article:
(E)-1,3-Dodecadien-1-yl acetate, an insect sex pheromone of the red bollworm moth, and (E,E)-1,3,5-undecatriene, a component of Dictyopteris and Galbanum, were synthesized in a highly stereo- and regioselective manner from allyl and pentadienyl dithiocarbamates, resp., by α-alkylation, rearrangement to the γ-alkyl derivative, reaction with Me3SiCH2I, and oxidative desulfurization. This study involved multiple reactions and reactants, such as (E)-Dodeca-9,11-dien-1-yl acetate (cas: 50767-78-7Recommanded Product: (E)-Dodeca-9,11-dien-1-yl acetate).
(E)-Dodeca-9,11-dien-1-yl acetate (cas: 50767-78-7) belongs to esters. Carboxylic acid esters of low molecular weight are colourless, volatile liquids with pleasant odours, slightly soluble in water. Cyclic esters are called lactones, regardless of whether they are derived from an organic or inorganic acid. One example of an organic lactone is γ-valerolactone.Recommanded Product: (E)-Dodeca-9,11-dien-1-yl acetate
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics