Reaction between (Z)‑Arylchlorooximes and α‑Isocyanoacetamides: A Procedure for the Synthesis of Aryl-α-ketoamide Amides
(Z)-Arylchlorooximes and α-isocyanoacetamides undergo a smooth reaction to produce 1,3-oxazol-2-oxime derivatives in good yields. Opening of the oxazole ring and deoximation reaction give a facile access to aryl-α-ketoamide amides, a class of privileged scaffolds in medicinal chemistry and important...
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Veröffentlicht in: | Journal of organic chemistry 2014-07, Vol.79 (13), p.6006-6014 |
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Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | (Z)-Arylchlorooximes and α-isocyanoacetamides undergo a smooth reaction to produce 1,3-oxazol-2-oxime derivatives in good yields. Opening of the oxazole ring and deoximation reaction give a facile access to aryl-α-ketoamide amides, a class of privileged scaffolds in medicinal chemistry and important synthetic intermediates in organic chemistry. |
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ISSN: | 0022-3263 1520-6904 |
DOI: | 10.1021/jo5005444 |