100298-06-4

Upstream product

• 79289-32-0 1-(diphenylmethylene)-4-methyl-3-oxo-1,2-diazetidinium hydroxide, inner salt 
• 1826-67-1 vinyl magnesium bromide 
• 74-88-4 methyl iodide 
• 100297-92-5 1-(1,1-diphenylprop-2-en-1-yl)-4-methyl-1,2-diazetidin-3-one 

Relevant academic research and scientific papers

Synthesis and R eactions of Some 2,2-Disubstitued 1,2-Diazetidin-3-ones: An Intramolecular Aldol Approach to Bicyclic Systems

Several procedures have been developed for alkylation at N-2 of a variety of 1,2-diazetidin-3-ones with N-1 substituent carrying an olefinic bond.Ozonolysis yielded aldehydes which were subjected to aldol cyclization conditions.The products proved to be rearranged bicyclic products arising from intramolecular ring opening of the 1,2-diazetidin-3-one lactam bond by the secondary hydroxyl group formed in the aldol reaction.