253445-79-3Relevant academic research and scientific papers
Synthesis, reactivity and biochemical evaluation of 1,3- substituted azetidin-2-ones as enzyme inhibitors
Beauve, Cecile,Bouchet, Michele,Touillaux, Roland,Fastrez, Jacques,Marchand-Brynaert, Jacqueline
, p. 13301 - 13320 (2007/10/03)
A series of monocyclic azetidinones were prepared, bearing, at position C-3, an acetylamino or a bromo substituent, at position N-1, a carboxymethyl group protected as p-nitrobenzyl ester (PNB) and α-functionalized with a potential leaving group (LG). The
