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- W2155103634 abstract "The first enantioselective aminolysis of aromatic trans-2,3-epoxy sulfonamides has been accomplished, which was efficiently catalyzed by a Gd-N,N'-dioxide complex. Under the directing effect of the sulfonamide moiety the ring-opening reaction proceeded selectively at the C-3 position in a highly enantioselective manner furnishing various Ts- and SES-protected 3-amino-3-phenylpropan-2-olamines as products." @default.
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- W2155103634 date "2015-06-08" @default.
- W2155103634 modified "2023-10-18" @default.
- W2155103634 title "Gadolinium-Catalyzed Regio- and Enantioselective Aminolysis of Aromatic<i>trans</i>-2,3-Epoxy Sulfonamides" @default.
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- W2155103634 doi "https://doi.org/10.1002/anie.201503391" @default.
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