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Article

Efficient Synthesis of Nα,N-Disubstituted α-Aminocarbohydroxamic Acids

by
Geffken Detlef
*,
Ploetz Alf
and
Zydowitz Hans v.
Department of Pharmaceutical Chemistry, University of Hamburg, Bundesstrasse 45,20 146 Hamburg, Germany
*
Author to whom correspondence should be addressed.
Sci. Pharm. 2002, 70(4), 325-330; https://doi.org/10.3797/scipharm.aut-02-31
Submission received: 19 August 2002 / Revised: 17 September 2002 / Accepted: 17 September 2002 / Published: 24 November 2002

Abstract

The title compounds 3 can be prepared in good yields by the reaction of N-substituted α-chlorocarbohydroxarnic acids 2 and primary amines in dirnethylacetarnide as solvent.
Keywords: N-subst ituted a-chlorocarbohydroxamic acids, primary amines, dimethylacetarnide, Nα,N-disubstituted α-arninocarbohydroxamic acids N-subst ituted a-chlorocarbohydroxamic acids, primary amines, dimethylacetarnide, Nα,N-disubstituted α-arninocarbohydroxamic acids

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MDPI and ACS Style

Detlef, G.; Alf, P.; Hans v., Z. Efficient Synthesis of Nα,N-Disubstituted α-Aminocarbohydroxamic Acids. Sci. Pharm. 2002, 70, 325-330. https://doi.org/10.3797/scipharm.aut-02-31

AMA Style

Detlef G, Alf P, Hans v. Z. Efficient Synthesis of Nα,N-Disubstituted α-Aminocarbohydroxamic Acids. Scientia Pharmaceutica. 2002; 70(4):325-330. https://doi.org/10.3797/scipharm.aut-02-31

Chicago/Turabian Style

Detlef, Geffken, Ploetz Alf, and Zydowitz Hans v. 2002. "Efficient Synthesis of Nα,N-Disubstituted α-Aminocarbohydroxamic Acids" Scientia Pharmaceutica 70, no. 4: 325-330. https://doi.org/10.3797/scipharm.aut-02-31

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