Issue 0, 1974

2-Amino-alcohols from α-amino-acids: a single-step mild procedure

Abstract

α-Amino-acids are reduced by diborane in anhydrous tetrahydrofuran to 2-amino-alcohols. Substituted halogenophenylalanines are reduced in good yield without hydrogenolysis of the halogen–carbon bond.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1974, 191-192

2-Amino-alcohols from α-amino-acids: a single-step mild procedure

M. Anhoury, M. Arickx, P. Crooy, R. De Neys and J. Eliaers, J. Chem. Soc., Perkin Trans. 1, 1974, 191 DOI: 10.1039/P19740000191

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