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Synlett 1991; 1991(4): 229-230
DOI: 10.1055/s-1991-20687
DOI: 10.1055/s-1991-20687
letter
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved.
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data processing and storage.C-Alkylation of Dianions of β-(Isopropylamino)-α,β-enones
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Publikationsverlauf
Publikationsdatum:
07. März 2002 (online)

A new alkylation method of enaminones (1-aryl-3-(isopropylamino)-2-buten-1-ones) via addition of electrophiles to dianions of β-(isopropylamino)-α, β-enones, generated by treatment with 2.5 equivalents of 2,2,6,6-tetramethylpiperidinolithium, is reported. The reaction works well with alkyl halides and aldehydes while poor yields are obtained from ketones.