172265-19-9Relevant academic research and scientific papers
N-bromoamides as versatile catalysts for aziridination of olefins using chloramine-T
Thakur, Vinay V.,Sudalai
, p. 989 - 992 (2007/10/03)
N-Bromoamides catalyze effectively the aziridination of electron-deficient as well as electron-rich olefins using chloramine-T (N-chloro-N-sodio-p-toluenesulfonamide) as a nitrogen source under ambient conditions to afford the corresponding aziridines in
Pyridinium hydrobromide perbromide: A versatile catalyst for aziridination of olefins using chloramine-T
Ali, Sayyed Iliyas,Nikalje, Milind D.,Sudalai
, p. 705 - 707 (2008/02/12)
Formula presented Pyridinium hydrobromide perbromide (PyHBr3) catalyzes effectively the aziridination of electron-deficient as well as electron-rich olefins using Chloramine-T (N-chloro-N-sodio-p-toluenesulfonamide) as a nitrogen source to afford the corr
Reduction of 2-acylaziridines by samarium(II) iodide. An efficient and regioselective route to β-amino carbonyl compounds
Molander, Gary A.,Stengel, Peter J.
, p. 8887 - 8912 (2007/10/03)
A convenient method for the reduction of 2-acylaziridines, aziridine-2- carboxylates and aziridine-2-carboxamides is described. The reduction of all of the substrates examined was extremely rapid and highly regioselective, giving rise to β-amino carbonyl compounds. This method appears to be general for all of the classes of aziridines mentioned above, and also tolerates a variety of nitrogen protecting groups.
