- catalytic conjugate addition
- Макаров: каталитическое сопряжённое присоединение
Универсальный англо-русский словарь. Академик.ру. 2011.
catalytic conjugate addition
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Boronic acid — The general structure of a boronic acid, where R is a substituent. A boronic acid is an alkyl or aryl substituted boric acid containing a carbon–boron bond belonging to the larger class of organoboranes. Boronic acids act as Lewis acids. Their… … Wikipedia
Organocopper compound — Lithium diphenylcuprate etherate dimer from crystal structure … 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
Michael reaction — The Michael reaction or Michael addition is the nucleophilic addition of a carbanion or another nucleophile[1][2][3] to an alpha, beta unsaturated carbonyl compound. It belongs to the larger class of conjugate additions. This is one of the most… … Wikipedia
Nazarov cyclization reaction — The Nazarov cyclization reaction (often referred to as simply the Nazarov cyclization) is a chemical reaction used in organic chemistry for the synthesis of cyclopentenones. The reaction is typically divided into classical and modern variants,… … Wikipedia
Radical (chemistry) — Free radical redirects here. For other uses, see Free radical (disambiguation). Moses Gomberg (1866 1947), the founder of radical chemistry Radicals (often referred to as free radicals) are atoms, molecules, or ions with unpaired electrons on an… … Wikipedia
Epoxide — A generic epoxide. An epoxide is a cyclic ether with three ring atoms. This ring approximately defines an equilateral triangle, which makes it highly strained. The strained ring makes epoxides more reactive than other ethers. Simple epoxides are… … Wikipedia
Baylis–Hillman reaction — The Baylis–Hillman reaction is an organic reaction of an aldehyde and an α,β unsaturated electron withdrawing group catalyzed by DABCO (1,4 diazabicyclo[2.2.2]octane) to give an allylic alcohol.[1][2] This reaction is also known as the… … Wikipedia
Danishefsky Taxol total synthesis — overview from raw material perspective The Danishefsky Taxol total synthesis in organic chemistry is an important third Taxol synthesis published by the group of Samuel Danishefsky in 1996 [1] two years after the first two efforts … Wikipedia
Diels–Alder reaction — Named after Otto Paul Hermann Diels Kurt Alder Reaction type Cycloaddition Reaction … Wikipedia
Diels-Alder reaction — The Diels Alder reaction is an organic chemical reaction (specifically, a cycloaddition) between a conjugated diene and a substituted alkene, commonly termed the dienophile, to form a substituted cyclohexene system. [cite journal author = Diels,… … Wikipedia
