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• W2177255225 endingPage "2011" @default.
• W2177255225 startingPage "2007" @default.
• W2177255225 abstract "An expeditious synthetic method of 3-arylidenelactams was developed starting from N-tosylaziridines, which were made from the reaction of N-tosylimines and cinnamyl bromides by using the sulfur ylide chemistry. The regioselective ring-opening reaction of N-tosylaziridines with anilines, as external nucleophiles, and the following lactamization afforded 3-arylidenelactams. In the absence of external nucleophiles, intramolecular lactonization occurred to afford 3-arylidenelactones." @default.
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• W2177255225 date "2007-03-01" @default.
• W2177255225 modified "2023-09-23" @default.
• W2177255225 title "Expeditious synthesis of 3-arylidenelactams and 3-arylidenelactones from N-tosylaziridine derivatives" @default.
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• W2177255225 doi "https://doi.org/10.1016/j.tetlet.2007.01.062" @default.
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