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A selective reductive amination of aldehydes by the use of Hantzsch dihydropyridines as reductant
Authors:Takashi Itoh
Institution:School of Pharmaceutical Sciences, Showa University, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo 142-8555, Japan
Abstract:Direct reductive amination of an aldehyde was carried out using a Hantzsch dihydropyridine as the reductant in the presence of a catalytic amount of scandium triflate. The reaction was highly selective towards aldehydes over ketones, and other reducible functional groups did not affect the reaction.
Keywords:Aldehyde  Ketone  Direct reductive amination  Imine  Hantzsch dihydropyridine  Scandium (III) triflate  Lewis acid
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