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 |
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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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