Synthesis and Structure of 5-Aryl-4-[hydroxyethyl]pyrrolidine-2,3- diones

The reactions of tryptamine with aromatic aldehyde and methyl benzoylpyruvate at room temperature leads to the formation of 5-aryl-4-[hydroxy(phenyl)Methylene]-1-[2-(1H-indol-3-yl)ethyl]pyrrolidine-2,3-diones. Keywords: heterocyclic analogues of N,N-dimethyltryptamine, 5-aryl-1-[2-(1H-indol-3-yl)eth...

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Veröffentlicht in:Russian journal of general chemistry 2019-11, Vol.89 (11), p.2196
Hauptverfasser: Gein, V.L, Varkentin, L.I, Kazantseva, M.I, Dmitriev, M.V, Yankin, A.N
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container_title Russian journal of general chemistry
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creator Gein, V.L
Varkentin, L.I
Kazantseva, M.I
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Yankin, A.N
description The reactions of tryptamine with aromatic aldehyde and methyl benzoylpyruvate at room temperature leads to the formation of 5-aryl-4-[hydroxy(phenyl)Methylene]-1-[2-(1H-indol-3-yl)ethyl]pyrrolidine-2,3-diones. Keywords: heterocyclic analogues of N,N-dimethyltryptamine, 5-aryl-1-[2-(1H-indol-3-yl)ethyl]pyrrolidine-2,3diones DOI: 10.1134/S1070363219110057
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subjects Aldehydes
Tryptophan
title Synthesis and Structure of 5-Aryl-4-[hydroxyethyl]pyrrolidine-2,3- diones
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