162900-97-2Relevant academic research and scientific papers
STEREOSELECTIVE ELECTROPHILIC HYDROXYLATION AT C-3 OF 2-AZETIDINONES
Annunziata, Rita,Benaglia, Maurizio,Cinquini, Mauro,Cozzi, Franco,Scolaro, Alessandra
, p. 65 - 68 (2007/10/02)
The enolates derived from 4-substituted-2-azetidinones react with an N-sulphonyloxaziridine to afford trans-3-hydroxy-substituted β-lactams in a completely stereoselective fashion and in moderate yields.Two examples of electrophilic sulphenylation and ami
