1082763-32-3Relevant academic research and scientific papers
The preparation of stable aziridinium ions and their ring-openings
Kim, Yongeun,Ha, Hyun-Joon,Yun, Sae Young,Lee, Won Koo
supporting information; experimental part, p. 4363 - 4365 (2009/03/12)
The reaction of enantiomerically pure 2-substituted 1-phenylethyl-aziridine with methyl trifluoromethanesulfonate generated a stable methylaziridinium ion, which was reacted with various external nucleophiles, including nitrile, to yield synthetically valuable and optically pure acyclic amine derivatives in a completely regio- and stereoselective manner. The Royal Society of Chemistry.
