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Synthesis 1994; 1994(7): 695-697
DOI: 10.1055/s-1994-25549
DOI: 10.1055/s-1994-25549
short paper
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved.
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data processing and storage.Regiospecific Synthesis of α-Amino Keto Acetals (β,β-Dialkoxyamines)
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Publikationsdatum:
17. September 2002 (online)
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α-Amino keto acetals (β,β-dialkoxyamines) are synthesized in a regiospecific way by the reaction of α-bromo-α-chloro ketimines with sodium borohydride in methanol. As α-bromo-α-chloro ketimines are formed regiospecifically from α,α-dihalogenated ketones, derived from the corresponding ketones, this methodology entails a regiospecific synthesis of α-amino keto acetals from ketones.