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asymmetric reduction

См. также в других словарях:

  • Asymmetric induction — (also enantioinduction) in stereochemistry describes the preferential formation in a chemical reaction of one enantiomer or diastereoisomer over the other as a result of the influence of a chiral feature present in the substrate, reagent,… …   Wikipedia

  • 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 federalism — or asymmetrical federalism is found in a federation in which different constituent states possess different powers: one or more of the states has considerably more autonomy than the other substates, although they have the same constitutional… …   Wikipedia

  • Asymmetric catalytic reduction — is the use of various chiral catalysts to reduce a prochiral organic compound to obtain a chiral product. This is one of the several techniques used in chiral synthesis.Typically, a transition metal is used with a bulky chiral ligand to such that …   Wikipedia

  • Meerwein–Ponndorf–Verley reduction — The Meerwein Ponndorf Verley (MPV) Reduction in organic chemistry is the reduction of ketones and aldehydes to their corresponding alcohols utilizing aluminumalkoxide catalysis in the presence of a sacrificial alcohol[1]. The beauty in the MPV… …   Wikipedia

  • Corey-Itsuno reduction — The Corey Itsuno Reduction, also known as the Corey Bakshi Shibata (CBS) reduction, is a chemical reaction in which an achiral ketone is enantioselectively reduced to produce the corresponding chiral, non racemic alcohol. The oxazaborolidine… …   Wikipedia

  • Noyori asymmetric hydrogenation — The Noyori asymmetric hydrogenation is a chemical reaction described as an asymmetric reduction of β keto esters.[1][2] …   Wikipedia

  • Midland Alpine Borane Reduction — The Midland Alpine borane reduction, or simply the Midland Reduction, allows for the asymmetric reduction of carbonyls (primarily ketones) to alcohols.[1] It was developed in the late 1970s by Professor M. Mark Midland at the University of… …   Wikipedia

  • Carbonyl reduction — synthesis of an alcohol by ester reduction Carbonyl reduction in organic chemistry is the organic reduction of any carbonyl group containing compound by a reducing agent. Typical carbonyl compounds are ketones , aldehydes, carboxylic acids and… …   Wikipedia

  • Galanthamine total synthesis — ; 2006; 106(1) pp 116 133; (Review) DOI|10.1021/cr040415t] The natural source of galantamine are certain species of daffodil and because these species are scarce and because the isolation of galanthamine from daffodil is expensive (a 1996 figure… …   Wikipedia

  • Alcohol — This article is about the generic chemistry term. For the kind of alcohol found in alcoholic beverages, see Ethanol. For beverages containing alcohol, see Alcoholic beverage. For other uses, see Alcohol (disambiguation) …   Wikipedia

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