Oxidation of β‑Ketoamides: The Synthesis of Vicinal Tricarbonyl Amides

A facile and direct oxidative reaction for the synthesis of vicinal tricarbonyl amides in moderate to excellent yields (53–88%) was developed starting from readily available β-ketoamides in the presence of phenyliodine­(III) bis­(trifluoroacetate). The resulting products possess significant syntheti...

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Veröffentlicht in:Journal of organic chemistry 2017-04, Vol.82 (7), p.3901-3907
Hauptverfasser: Liu, Yueyang, Zhang, Zhiguo, Wan, Yameng, Zhang, Guisheng, Li, Zhonglian, Bi, Jingjing, Ma, Nana, Liu, Tongxin, Liu, Qingfeng
Format: Artikel
Sprache:eng
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Zusammenfassung:A facile and direct oxidative reaction for the synthesis of vicinal tricarbonyl amides in moderate to excellent yields (53–88%) was developed starting from readily available β-ketoamides in the presence of phenyliodine­(III) bis­(trifluoroacetate). The resulting products possess significant synthetic potential, making this approach a valuable addition to the group of traditional methods already available for the preparation of these molecules.
ISSN:0022-3263
1520-6904
DOI:10.1021/acs.joc.6b03062