Catalytic, enantioselective synthesis of Boc-protected 1,2-amino alcohols through aminolysis of meso-epoxides with benzophenone imine

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Abstract

Aromatic meso-epoxides 3 have been ring-opened with benzophenone imine (2) using catalytic quantities of the chiral scandium bipyridine complex 1a to furnish Boc-protected 1,2-amino alcohols 5 in good yields and enantioselectivities after acidic hydrolysis and Boc-protection. © ARKAT USA, Inc.

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APA

Mai, E., & Schneider, C. (2008). Catalytic, enantioselective synthesis of Boc-protected 1,2-amino alcohols through aminolysis of meso-epoxides with benzophenone imine. Arkivoc, 2008(16), 216–222. https://doi.org/10.3998/ark.5550190.0009.g20

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