115142-70-6

Upstream product

• 4702-13-0 N-phthaloylglycine 
• 108908-63-0 N-4-methoxyphenyl-α-methylcinnamylideneamine 
• 115142-70-6 cis-4-acetyl-1-(4-methoxyphenyl)-3-phthalimido-2-azetidinone 
• 84208-59-3 cis-1-(4-methoxyphenyl)-4-(α-methylstyryl)-3-phtalimido-2-azetidinone 
• 104-94-9 4-methoxy-aniline 
• 6780-38-7 N-phthaloylglycine chloride 

Downstream Products

• 114987-10-9 cis-4-acetoxy-1-(4-methoxyphenyl)-3-phthalimido-2-azetidinone 
• 115142-70-6 trans-4-acetyl-1-(4-methoxyphenyl)-3-phthalimido-2-azetidinone 
• 114987-10-9 trans-4-acetoxy-1-(4-methoxyphenyl)-3-phthalimido-2-azetidinone 
• 115957-20-5 1-(4-methoxyphenyl)-3-phthalimidoazetidin-2-one 

Relevant academic research and scientific papers

Leuckart Reductive Amination of a 4-Acetylazetidinone using Microwave Technology

The reductive amination of cis-4-acetyl-1-(4-methoxyphenyl)-3-phthalimidoazetidinone has been studied under different conditions.The reaction leads to a mixture of three compounds that have been characterized by chemical correlation.

Preparation of 4-Unsubstituted β-Lactams from 4-Acetoxyazetidin-2-ones.A Formal Approach to Monobactams and Nocardicins

The synthesis of 4-unsubstituted azetidin-2-ones is described.Treatment of Schiff bases derived from α-methylcinnamaldehyde and amines with acetic acids in the presence of phenyl dichlorophosphate and triethylamine followed by ozonolysis of the resulting