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Synthesis 2006(10): 1625-1630
DOI: 10.1055/s-2006-926457
DOI: 10.1055/s-2006-926457
PAPER
© Georg Thieme Verlag Stuttgart · New York
Aminoalkylation of ‘Push-Pull’ Enamines Having a Methyl Group at the α-Position with Imines of Methyl 3,3,3-Trifluoropyruvate
Weitere Informationen
Received
12 December 2005
Publikationsdatum:
27. April 2006 (online)
Publikationsverlauf
Publikationsdatum:
27. April 2006 (online)
Abstract
The reaction of ‘push-pull’ enamines having a methyl group at the α-position with imines of methyl 3,3,3-trifluoropyruvate was investigated. Structural sensitivity of the reaction was found and discussed. As a result, a set of β-dicarbonyl compounds bearing a protected amino acid moiety was obtained.
Key words
‘push-pull’ enamines - imines of methyl 3,3,3-trifluoropyruvate - aminoalkylation - protected amino acids
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