87568-43-2

Upstream product

• 228720-65-8 (+/-)-1-(4'-methoxyphenyl)-3-hydroxy-azetidin-2-one 
• 33692-63-6 dimethyl N-(para-methoxyphenyl)-dithio-carbonimidate 
• 142389-21-7 C₁₂H₁₇NOS₂ 
• 228720-64-7 1-(4'-methoxyphenyl)-3-acetoxy-azetidin-2-one 
• 228720-63-6 1-(4'-methoxy-phenyl)-3-acetoxy-4,4-bis(methylthio)azetidin-2-one 
• 228720-78-3 1-(4'-methoxyphenyl)-3-acetoxy-4,4-bis(ethylthio)azetidin-2-one 
• 7274-71-7 N-(4-methoxyphenyl)-2-methylacrylamide 
• 87568-30-7 1-(p-methoxyphenyl)-3-methyl-3-(phenylthio)azetidin-2-one 
• 87568-42-1 1-(p-methoxyphenyl)-3-methyl-3-(phenylsulfinyl)azetidin-2-one 
• 69193-56-2 1-(4-methoxyphenyl)-3-methylideneazetidin-2-one 
• 20109-30-2 6,6'-dimethyl-2,2'-sulfanediyl-di-phenol 

Downstream Products

• 87568-46-5 3-(((benzyloxy)carbonyl)amino)-1-(p-methoxyphenyl)azetidin-2-one 
• 87568-45-4 3-amino-1-(p-methoxyphenyl)azetidin-2-one 
• 87568-44-3 1-(p-methoxyphenyl)azetidin-2-one 3-oxime 

Relevant academic research and scientific papers

Chemo-enzymatic synthesis of chiral 3-hydroxy-azetidin-2-ones

n-Tributyltin hydride reduction of 3-acetoxy-4,4-bis(alkylthio)- azetidin-2-ones 4a and 4b produces 4-unsubstituted azetidinone 5 and 4- alkylthio-azetidin-2-one 9 respectively. Azetidin-2,3-diones 8,11,13 which can be conveniently prepared by basic hydro

Ozonide reducing agent

The present invention provides an ozonide reducing agent for use in the ozonolysis reaction of an organic compound, the ozonide reducing agent finding wide applications, and being safe and inexpensive from a commercial viewpoint and easy to treat for disp

Synthesis of β-lactam antibiotics by the sulfeno-cycloamination

A novel efficient beta -lactam synthesis was achieved by two successive processes (sulfeno-cycloamination), addition of phenysulfenyl chloride to alpha , beta -unsaturated amides followed by base treatment. Key synthetic intermediates of monobactams and nocardicin derivatives were obtained via this method. construction of the 1-carbapenam ring system by the sulfenocycloamination is also described.