103247-89-8Relevant articles and documents
The acid-mediated ring opening reactions of α-aryl-lactams
King, Frank D.,Caddick, Stephen
experimental part, p. 3244 - 3252 (2012/06/01)
4-Aryl-azetidin-2-ones (β-lactams) undergo ring opening with triflic acid to give cinnamamides which, in benzene, react further to give 3-aryl-3-phenyl-propionamides. Prolonged reaction times in benzene give 3,3-diphenyl-propionamide via an aryl/phenyl ex
The Reaction of 4-Phenyl-2-azetidinone with Aldehydes
Bergmann, Hans-Joachim,Otto, Hans-Hartwig
, p. 216 - 226 (2007/10/02)
The title compound 1 reacts with aliphatic aldehydes to yield N-(1-hydroxyalkyl) derivatives 5, which can be dehydrated to N-vinyl-β-lactams 6.The reaction of 1 with aromatic aldehydes gives amidols 9, from which the derivatives 10 are obtained by acylation.