Re, Rebecca N.; Proessdorf, Johanna C.; La Clair, James J.; Subileau, Maeva; Burkart, Michael D. published an article in 2019, the title of the article was Tailoring chemoenzymic oxidation via in situ peracids.Recommanded Product: 2873-29-2 And the article contains the following content:
Epoxidation chem. often suffers from the challenging handling of peracids and thus requires in situ preparation Here, we describe a two-phase enzymic system that allows the effective generation of peracids and directly translate their activity to the epoxidation of olefins. We demonstrate the approach by application to lipid and olefin epoxidation as well as sulfide oxidation These methods offer useful applications to synthetic modifications and scalable green processes. The experimental process involved the reaction of (2R,3S,4R)-2-(Acetoxymethyl)-3,4-dihydro-2H-pyran-3,4-diyl diacetate(cas: 2873-29-2).Recommanded Product: 2873-29-2
The Article related to chemoenzymic oxidation peracid olefin lipid epoxidation, Biochemical Methods: Reagents and other aspects.Recommanded Product: 2873-29-2
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics