Abstract
Abstract The asymmetric nucleophilic addition of Reformatsky-type reagent to imines, which were prepared from aldehydes and 2-aminophenols, was achieved by the use of diisopropyl (R, R)-tartrate as a chiral auxiliary to afford the corresponding β-amino acid ester derivatives with excellent enantioselectivities. In order to realize reproducible higher stereoselection, the addition of a small amount of water was crucial.
Full Text 
Sign-in/Register to access full text options
Sign-in/Register to access full text options 
Published version (
Free)
Free) 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call
