Catalytic allylic oxidation with a recyclable, fluorous seleninic acid was written by Crich, David;Zou, Yekui. And the article was included in Organic Letters in 2004.Formula: C12H18O3 The following contents are mentioned in the article:
In conjunction with iodoxybenzene as reoxidant, perfluorooctylseleninic acid (I) catalyzed the allylic oxidation of alkenes to enones, in moderate to good yield. After a reductive workup with sodium metabisulfite, the catalyst was recovered by fluorous extraction in the form of bis(perfluorooctyl) diselenide, which, itself, serves as a convenient catalyst precursor. 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. Volatile esters with characteristic odours are used in synthetic flavours, perfumes, and cosmetics. Certain volatile esters are used as solvents for lacquers, paints, and varnishes. Liquid esters of low volatility serve as softening agents for resins and plastics. Esters also include many industrially important polymers. Polymethyl methacrylate is a glass substitute sold under the names Lucite and Plexiglas; polyethylene terephthalate is used as a film (Mylar) and as textile fibres sold as Terylene, Fortrel, and Dacron.Formula: C12H18O3
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics