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Zincke reaction - Wikipedia The Zincke reaction is an organic reaction, named after Theodor Zincke, in which a pyridine is transformed into a pyridinium salt by reaction with 2,4-dinitro-chlorobenzene and a primary amine [1][2][3][4] The Zincke reaction should not be confused with the Zincke-Suhl reaction or the Zincke nitration
Zincke aldehyde - Wikipedia Zincke aldehydes, or 5-aminopenta-2,4-dienals, are the product of the reaction of a pyridinium salt with two equivalents of any secondary amine, followed by basic hydrolysis
Zincke reaction - Springer The Zincke reaction is an overall amine exchange process that converts N -(2,4- dinitrophenyl)pyridinium salts, known as Zincke salts, to N -aryl or N -alkyl pyri- diniums upon treatment with the appropriate aniline or alkyl amine
Unraveling the Mechanism of Cascade Reactions of Zincke Aldehydes The thermal pericyclic cascade rearrangement of Zincke aldehydes (5- (dialkylamino)-2,4-pentadienals) to afford Z -α,β,γ,δ-unsaturated amides discovered by the Vanderwal group has been studied in depth using quantum mechanical methods
Zincke Reaction - SynArchive The Zincke reaction is the reaction between 1-(2,4-dinitrophenyl)pyridinium salts and amines Primary amines yield pyridinium salts while secondary amines yield 5-(dialkylamino)penta-2,4-dienals (Zincke aldehydes)
Zincke reaction - Wikiwand The Zincke reaction is an organic reaction, named after Theodor Zincke, in which a pyridine is transformed into a pyridinium salt by reaction with 2,4-dinitro-chlorobenzene and a primary amine The Zincke reaction should not be confused with the Zincke-Suhl reaction or the Zincke nitration
Zincke reaction, pyridinium salts - Big Chemical Encyclopedia The Zincke reaction is an overall amine exchange process that converts N- 2,A-dinitrophenyl)pyridinium salts, known as Zincke salts, to A -aryl or A -alkyl pyridiniums upon treatment with the appropriate aniline or alkyl amine