An efficient chemo‐ and stereoselective synthesis of enaminones and enaminoesters using (bromodimethyl)sulfonium bromide under solvent‐free conditions

(Bromodimethyl)sulfonium bromide has efficiently been employed for chemo- and stereoselective conversions of β-dicarbonyl compounds into β-enaminones and β-enaminoesters by a treatment with amines at room temperature under solvent-free conditions. © 2008 Wiley Periodicals, Inc. Heteroatom Chem 19:630–633, 2008; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.20477

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