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Asymmetric synthesis of fagomine
Affiliation:University of Toyama, Department of Chemistry, Gofuku3190, Toyama 930-8555, Japan
Abstract:We report an asymmetric synthesis of the alkaloid fagomine, which is an inhibitor of mammalian α-glucosidase and β-galactosidase, by means of Sharpless asymmetric dihydroxylation and Pd(II)-catalyzed cyclization, starting from 3-(t-butoxylcarbonylamino)propanol.
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