Oxidation of olefins with 2-pyridineseleninic anhydride was written by Barton, Derek H. R.;Crich, David. And the article was included in Tetrahedron in 1985.Recommanded Product: 37905-02-5 The following contents are mentioned in the article:
2-Pyridineseleninic anhydride (I) prepared in situ by oxidation of the corresponding diselenide with iodoxybenzene, is an efficient reagent for the conversion of olefins to unsaturated ketones with retention of the original position of the double bond. Thus, oxidation of β-pinene gave 95% (+)-pinocarvone. This reagent is much more reactive towards olefins than benzeneseleninic anhydride. This study involved multiple reactions and reactants, such as (2E,6E)-3,7-Dimethyl-8-oxoocta-2,6-dien-1-yl acetate (cas: 37905-02-5Recommanded Product: 37905-02-5).
(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. Polyesters are important plastics, with monomers linked by ester moieties. Because of their lack of hydrogen-bond-donating ability, esters do not self-associate. Consequently, esters are more volatile than carboxylic acids of similar molecular weight.Recommanded Product: 37905-02-5
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics