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Synthesis 2005(5): 725-730
DOI: 10.1055/s-2005-861803
DOI: 10.1055/s-2005-861803
PAPER
© Georg Thieme Verlag Stuttgart · New YorkAn Efficient and Diastereoselective Synthesis of trans β-Lactams and β-Aminocarbonyl Compounds
Weitere Informationen
Received
13 September 2004
Publikationsdatum:
09. Februar 2005 (online)
Publikationsverlauf
Publikationsdatum:
09. Februar 2005 (online)
Abstract
Efficient and diastereoselective syntheses of trans β-lactams and anti β-aminocarbonyl compounds from carboximide 1 and imines 2 under the classical Reformatsky reaction conditions are described. An enolate-imine mechanism has been proposed for this reaction.
Key words
β-lactams - imines - Reformatsky reaction - β-aminocarbonyl compounds
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