Enantioselective organocatalytic transfer hydrogenation of α-imino esters by utilization of benzothiazoline as highly efficient reducing agent

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Abstract

Benzothiazoline was employed as an efficient and versatile reducing agent for the chiral phosphoric acid-catalyzed transfer hydrogenation of α-imino esters. The corresponding α-amino esters were furnished with excellent enantioselectivities. Novel and readily removable benzothiazolines bearinga hydroxy group were also investigated. © 2010 Wiley-VCH Verlag GmbH&Co. KGaA, Weinheim.

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Zhu, C., & Akiyama, T. (2010). Enantioselective organocatalytic transfer hydrogenation of α-imino esters by utilization of benzothiazoline as highly efficient reducing agent. Advanced Synthesis and Catalysis, 352(11–12), 1846–1850. https://doi.org/10.1002/adsc.201000328

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