Issue 8, 1974

Reduction of β-nitrostyrene with sodium bis-(2-methoxyethoxy)-aluminium dihydride. A convenient route to substituted phenylisopropylamines

Abstract

β-Arylethylamines may be generated conveniently and in good yields by reduction of the corresponding styryl precursors with ‘Redal’[sodium bis-(2-methoxyethoxy)aluminium dihydride].

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1974, 307-308

Reduction of β-nitrostyrene with sodium bis-(2-methoxyethoxy)-aluminium dihydride. A convenient route to substituted phenylisopropylamines

J. R. Butterick and A. M. Unrau, J. Chem. Soc., Chem. Commun., 1974, 307 DOI: 10.1039/C39740000307

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