ChemInform Abstract: Synthesis of 2-Aryl-3-(2-cyanoethyl)aziridines and Their Chemical and Enzymatic Hydrolysis Towards γ-Lactams and γ-Lactones

The title compounds (IV) are transformed into variable mixtures of 4‐[aryl(alkylamino)methyl]butyrolactones and 5‐[aryl(hydroxy)methyl]pyrrolidin‐2‐ones by KOH‐mediated hydrolysis of the cyano group, followed by ring expansion.

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Veröffentlicht in:ChemInform 2015-07, Vol.46 (27), p.no-no
Hauptverfasser: Mollet, Karen, Decuyper, Lena, Vander Meeren, Saskia, Piens, Nicola, De Winter, Karel, Desmet, Tom, D'hooghe, Matthias
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container_title ChemInform
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creator Mollet, Karen
Decuyper, Lena
Vander Meeren, Saskia
Piens, Nicola
De Winter, Karel
Desmet, Tom
D'hooghe, Matthias
description The title compounds (IV) are transformed into variable mixtures of 4‐[aryl(alkylamino)methyl]butyrolactones and 5‐[aryl(hydroxy)methyl]pyrrolidin‐2‐ones by KOH‐mediated hydrolysis of the cyano group, followed by ring expansion.
doi_str_mv 10.1002/chin.201527134
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subjects aziridine derivatives
biochemical syntheses
biochemical syntheses, microbiological syntheses
furan derivatives
mechanochemistry
microbiological syntheses
microwave chemistry
microwave chemistry, sonochemistry, mechanochemistry
pyrrole derivatives
ring contraction
ring expansion
sonochemistry
title ChemInform Abstract: Synthesis of 2-Aryl-3-(2-cyanoethyl)aziridines and Their Chemical and Enzymatic Hydrolysis Towards γ-Lactams and γ-Lactones
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