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- W2147134920 abstract "The reaction between triphenylphosphine, dialkylacetylenedicarboxylates, and N-benzoyl thiourea derivatives leads to intermediates such as vinyltriphenylphosphonium salts, which undergo Michael addition to produce the highly functionalized phosphorus ylides containing alkyl groups in excellent yields. Using silica gel as a catalyst, the conversion of the stabilized phosphorus ylides to benzo[e][1,3]thiazocin derivatives in solvent free conditions at 90°C in fairly high yields is achieved." @default.
- W2147134920 created "2016-06-24" @default.
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- W2147134920 date "2010-08-25" @default.
- W2147134920 modified "2023-10-17" @default.
- W2147134920 title "Silica-Gel–Catalyzed Conversion of Stabilized Phosphorus Ylides to Benzo[<i>e</i>][1,3]Thiazocin Derivatives" @default.
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- W2147134920 doi "https://doi.org/10.1080/10426500903376147" @default.
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