126748-42-3Relevant articles and documents
Nitrosative Deamination of 1-Aminoazetidin-2-ones. An Entry to N-Unsubstituted β-Lactams
White,, James D.,Perri, Steven T.,Toske, Steven G.
, p. 433 - 436 (2007/10/02)
Nitrosative deamination of 1-aminoazetidin-2-ones was carried out with diphenylnitrosamine to give the N-unsubstituted systems, thus completing a route to β-lactams by photochemical ring contraction of pyrazolidin-3-ones.Key Words: β-Lactams; Diphenylnitrosamine; Deamination