93692-57-0Relevant academic research and scientific papers
A trans-stereoselective synthesis of 3-halo-4-alkyl(aryl)-NH-azetidin-2-ones
Bandini, Elisa,Favi, Gianfranco,Martelli, Giorgio,Panunzio, Mauro,Piersanti, Giovanni
, p. 1077 - 1079 (2007/10/03)
Conrotatory ring closure of 1-halo-3-aza-4-alkyl-1,3-dienes in refluxing toluene gives rise to 3-halo-4-aryl-2-azetidinones in satisfactory yields. Dehalogenation of the resulting β-lactams by tris(trimethylsilyl)silane furnished 3-unsubstituted azetidino
