177963-03-0Relevant academic research and scientific papers
Lewis acid-mediated highly regioselective SN2-type ring-opening of 2-Aryl-N-tosylazetidines and aziridines by alcohols
Ghorai, Manas K.,Das, Kalpataru,Shukla, Dipti
, p. 5859 - 5862 (2007)
(Chemical Equation Presented) Lewis acid-mediated highly regioselective SN2-type ring-opening of 2-aryl-N-tosylazetidines with alcohols to afford various 1,3-amino ethers in excellent yields with good enantiomeric excess is described. Similar S
Asymmetric synthesis of β-alkoxy substituted phenethylamide analogs
Zaponakis,Katerinopoulos
, p. 3045 - 3048 (2007/10/03)
The enantioselective synthesis of beta-alkoxy substituted phenethylamines is described. The enantiomeric excess of the products ranges from 77 to 87%.
