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  1. Efficient asymmetric synthesis of N-protected-β-aryloxyamino acids via regioselective ring opening of serine sulfamidate carboxylic acid
  2. Catalytic asymmetric aminolactonization
  3. Asymmetric synthesis towards doxanthrine, a dopamine D1 full agonist
  4. A diastereoselective route to 2,5-diaryl-3,4-disubstituted tetrahydrofuran lignans: protection free synthesis of (+)-galbelgin and (+)-galbacin