Issue 15, 1977

Synthesis of amino-acids by electroreductive coupling of alkyl halides with Schiff's bases

Abstract

α-Methyl-α-amino-acids and phenylalanine have been synthesized in 36–86% yield by a route involving controlled potential cathodic reduction of alkyl halides in the presence of Schiff's bases in a non-aqueous catholyte.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1977, 1730-1733

Synthesis of amino-acids by electroreductive coupling of alkyl halides with Schiff's bases

T. Iwasaki and K. Harada, J. Chem. Soc., Perkin Trans. 1, 1977, 1730 DOI: 10.1039/P19770001730

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