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AUyl alcohols asymmetric epoxidation

The epoxidation of enones using chiral phase transfer catalysis (PTC) is an emerging technology that does not use transition metal catalysts. Lygo and To described the use of anthracenylmethyl derivatives of a cinchona alkaloid that are capable of catalyzing the epoxidation of enones with remarkable levels of asymmetric control and a one pot method for oxidation of the aUyl alcohol directly into... [Pg.25]

Enzymatic hydrolysis of AJ-acjiamino acids by amino acylase and amino acid esters by Hpase or carboxy esterase (70) is one kind of kinetic resolution. Kinetic resolution is found in chemical synthesis such as by epoxidation of racemic aUyl alcohol and asymmetric hydrogenation (71). New routes for amino acid manufacturing are anticipated. [Pg.279]


See other pages where AUyl alcohols asymmetric epoxidation is mentioned: [Pg.84]    [Pg.1048]    [Pg.224]   
See also in sourсe #XX -- [ Pg.7 , Pg.397 , Pg.406 , Pg.408 , Pg.417 ]




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