An efficient Sn(ii)-catalyzed one-pot synthesis of a 3-substituted azetidine-2,4-dione framework

A novel Sn(ii)-catalyzed tandem cyclization reaction of aromatic aldehydes with ethyl cyanoacetate has been achieved to afford a series of 3-substituted azetidine-2,4-diones in good to excellent yields. This protocol provides straightforward access to construct the azetidine core through sequential...

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Veröffentlicht in:Organic & biomolecular chemistry 2017-03, Vol.15 (11), p.2385-2391
Hauptverfasser: Chavan, Santosh S, Supekar, Mrudul V, Burate, Pralhad A, Rupanwar, Bapurao D, Shelke, Anil M, Suryavanshi, Gurunath
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Sprache:eng
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Zusammenfassung:A novel Sn(ii)-catalyzed tandem cyclization reaction of aromatic aldehydes with ethyl cyanoacetate has been achieved to afford a series of 3-substituted azetidine-2,4-diones in good to excellent yields. This protocol provides straightforward access to construct the azetidine core through sequential Knoevenagel condensation, hydration and the C-N cyclization reaction.
ISSN:1477-0520
1477-0539
DOI:10.1039/c7ob00294g