Synthesis of compounds with juvenile hormone activity. XVII. Stereoselective synthesis of dl-C17-Cecropia juvenile hormone was written by Mori, K.;Ohki, M.;Matsui, M.. And the article was included in Tetrahedron in 1974.Formula: C12H18O3 The following contents are mentioned in the article:
Me 12-homofarnesoate, whose conversion to the title hormone is documented, was prepared from EtCMe:CHCH2SPh by successive coupling with 8-tetrahydro-pyranyloxy-2,6-dimethylocta-2,6-trans,trans-dienyl bromide, removal of the tetrahydropyranyl and PhS groups, and oxidative esterification. This study involved multiple reactions and reactants, such as (2E,6E)-3,7-Dimethyl-8-oxoocta-2,6-dien-1-yl acetate (cas: 37905-02-5Formula: C12H18O3).
(2E,6E)-3,7-Dimethyl-8-oxoocta-2,6-dien-1-yl acetate (cas: 37905-02-5) belongs to esters. Esters perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Acyl chlorides and acid anhydrides alcoholysis is another way to produce esters. Acyl chlorides and acid anhydrides react with alcohols to produce esters. Anydrous conditions are recommended since both acyl chlorides and acid anhydrides react with water.Formula: C12H18O3
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics