A New Approach to the Synthesis of Optically Active Norephedrine, Norpseudoephedrine and Cathinone via Double Asymmetric Induction

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Abstract

New and facile synthetic routes for preparation of optically active norephedrine, norpseudoephedrine and cathinone with high optical purities via double asymmetric induction by employing asymmetric reduction of 2-N-protected amino (or azido)-1-phenylpropanone and 2-methanesulfonyloxy-1-phenylpropanone with CBS-catalyzed-borane and dIpc2BCl as chiral reducing agents are described.

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Kim, D. J., & Cho, B. T. (2003). A New Approach to the Synthesis of Optically Active Norephedrine, Norpseudoephedrine and Cathinone via Double Asymmetric Induction. Bulletin of the Korean Chemical Society, 24(11), 1641–1648. https://doi.org/10.5012/bkcs.2003.24.11.1641

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