Chemistry of phosphorus ylides 21 new route for the synthesis of azetidinones. Reaction of phosphonium ylides with benzil-, o-naphthoquinone-, and triketonemonoanils

✍ Scribed by Fouad M. Soliman; Medhat M. Said; Soher S. Maigali

• Publisher: John Wiley and Sons
• Year: 2005
• Tongue: English
• Weight: 113 KB
• Volume: 16
• Category: Article
• ISSN: 1042-7163
• DOI: 10.1002/hc.20144

✦ Synopsis

Active vinylidenetriphenylphosphoranes are nucleophilic reagents which can be considered as versatile synthons for the synthesis of new heterocycles. The active phosphacumulene ylides, namely N-phenylimino-2a, 2-oxo-2b or 2-thioxovinylidenetriphenylphosphoranes (2c), react with benzil-(1a,b), o-naphthoquinone-(8), or triketonemonoanils (11), to give the corresponding phenylimino-(3a, d, 9a, 12a), oxo-(3b, e, 9b, 12b), or thioxoazetidinones (3c, f, 9c, 12c), respectively, which constitute an important class of organic compounds with medicinal and biological importance. On the other hand, quinone monoanils 1a, 8, 11 can be converted by reaction with the stabilized alkylidenephosphoranes (5a-d), namely acetylmethylene-5a, methoxycarbonylmethylene-5b, ethoxycarbonylmethylene-5c, and benzoylmethylenetriphenylphosphorane 5d, into the phosphoranylidenes ( 7a-d, 10a-d, 13a-d). No reaction was observed between iminophosphorane ( 14) and the monoanil (11). The structures of the new products were assigned according to consistent analytical and spectroscopic data.