- asymmetric oxidation
- 不对称氧化
English-Chinese chemistry dictionary (英汉化学大词典). 2013.
English-Chinese chemistry dictionary (英汉化学大词典). 2013.
Asymmetric synthesis — Asymmetric synthesis, also called chiral synthesis, enantioselective synthesis or stereoselective synthesis, is organic synthesis which introduces one or more new and desired elements of chirality. [GoldBookRef|title=asymmetric synthesis| file =… … Wikipedia
Asymmetric catalytic oxidation — is a technique of oxidizing various substrates to give an enantiopure product using a catalyst.Reactions*Jacobsen epoxidation of alkenes using manganese salen complex and NaOCl *Sharpless epoxidation of allyl alcohols using titanium isopropoxide … Wikipedia
Oxidation with dioxiranes — refers to the introduction of oxygen into organic molecules through the action of a dioxirane. Dioxiranes are well known for their oxidation of alkenes to epoxides; however, they are also able to oxidize other unsaturated functionality,… … Wikipedia
Oxidation of primary alcohols to carboxylic acids — The oxidation of primary alcohols to carboxylic acids is an important oxidation reaction in organic chemistry. When a primary alcohol is converted to a carboxylic acid, the terminal carbon atom increases its oxidation state by four. Oxidants able … Wikipedia
Oppenauer oxidation — Oppenauer oxidation, named after Rupert Viktor Oppenauer,[1] is a gentle method for selectively oxidizing secondary alcohols to ketones. The reaction is the opposite of Meerwein Ponndorf Verley reduction. The alcohol is oxidized with aluminium… … Wikipedia
Sharpless asymmetric dihydroxylation — (also called the Sharpless bishydroxylation) is the chemical reaction of an alkene with osmium tetroxide in the presence of a chiral quinine ligand to form a vicinal diol.[1][2][3] … Wikipedia
Noyori asymmetric hydrogenation — The Noyori asymmetric hydrogenation is a chemical reaction described as an asymmetric reduction of β keto esters.[1][2] … Wikipedia
Baeyer-Villiger oxidation — The Baeyer Villiger oxidation is an organic reaction in which a ketone is oxidized to an ester by treatment with peroxy acids or hydrogen peroxide.cite journal | authorlink = Adolf von Baeyer | last = Baeyer | first = A. | coauthors = Villiger, V … Wikipedia
Lemieux-Johnson oxidation — The Lemieux Johnson oxidation is a chemical reaction named after its discoverers, R. U. Lemieux and W. S. Johnson, who published it in 1956. [cite journal author = Pappo, R.; Allen, D. S., Jr.; Lemieux, R. U.; Johnson, W. S. title = Osmium… … Wikipedia
Oxaziridine — Oxaziridine … Wikipedia
Acyloin — The structure of a typical acyloin. Acyloins (also referred to as ketols) are a class of organic compounds in organic chemistry sharing a common functional group consisting of a hydroxyl group placed on the α position of a carbonyl group.… … Wikipedia