115344-33-7Relevant academic research and scientific papers
AN AZIRIDINE ROUTE TO CHIRAL β-LACTAMS A NOVEL ENTRY TO (+)-THIENAMYCIN
Tanner, David,Somfai, Peter
, p. 1211 - 1214 (1987)
Enantiomerically pure 2,3-epoxy alcohols are transformed readily and stereospecifically to the corresponding aziridines, regioselective ring-opening of which allows subsequent conversion to chiral β-lactams suitable for elaboration to the title antibiotic
