167156-71-0Relevant articles and documents
Amphoteric amino aldehydes reroute the Aza-Michael reaction
Hili, Ryan,Yudin, Andrei K.
supporting information; experimental part, p. 16404 - 16406 (2010/02/15)
(Chemical Equation Presented) Amphoteric amino aldehydes, which exist as stable dimers, participate in an aza-Michael/aldol domino reaction with α,β-unsaturated aldehydes to afford stable 1,5-aminohydroxyaldehydes in high yields and diastereoselectivies.
Preparation of Optically Active Aziridine Carboxylates by Lipase-Catalyzed Alcoholysis
Martres, Monique,Gil, Gerard,Meou, Alain
, p. 8787 - 8790 (2007/10/02)
Aziridine carboxylates alcoholysis by lipases depends of the N-substituent.N-alkyl and N-aryl compounds have been resolved with medium to good enantiomeric purity by enzymatic alcoholysis catalyzed by pig pancreatic (PPL) or Candida cylindracea lipase (CC