40339-42-2

Upstream product

• 100-52-7 benzaldehyde 
• 104-94-9 4-methoxy-aniline 

Downstream Products

• 152511-66-5 3-(4-methoxy-phenyl)-2,5-diphenyl-3,4-dihydro-2H-imidazole-1-oxide 
• 81375-53-3 3-p-methoxyphenyl-6-methyl-2-phenyl-1,3-oxazin-4-one 
• 19340-68-2 1-(4-methoxy-phenyl)-4-phenyl-azetidin-2-one 
• 51527-45-8 1-(4-Methoxyphenyl)-3,4-diphenylazetidin-2-on 
• 79457-89-9 trans-α-Phenylzimtsaeure-(4-methoxyanilid) 
• 22086-00-6 3,3-dichloro-1-p-methoxyphenyl-4-phenyl-2-azetidinone 
• 17377-95-6 benzyl(4-methoxyphenyl)amine 
• 61458-06-8 (+/-)-cis-1-(4-methoxyphenyl)-2-oxo-4-phenylazetidin-3-yl-isoindoline-1,3-dione 
• 802-49-3 3-(4-methoxyphenylamino)-1,3-diphenyl-1-propanone 
• 5568-58-1 4-ethoxy-6-methoxy-2-phenyl-1,2,3,4-tetrahydro-quinoline 
• 131968-76-8 (+/-)-(3R,4S)-3-acetoxy-N-(4-methoxyphenyl)-4-phenylazetidin-2-one 
• 128897-27-8 1-(4-methoxyphenyl)-3,3-dimethyl-4-phenyl-2-azetidinone 
• 94612-26-7 1-p-Anisyl-3-thiophenoxy-3-chloro-4-phenylazetidine-2-one 
• 94612-33-6 1-(4-methoxyphenyl)-4-phenylazetidine-2,3-dione 

Relevant academic research and scientific papers

Arthrobacter sp.: a lipase of choice for the kinetic resolution of racemic arylazetidinone precursors of taxanoid side chains

The native strain of Arthrobacter sp. (MTCC 5125) bearing a lipase has been found to be the most effective in the kinetic resolution of racemic arylazetidinones for producing cis-(3R,4S)-3-acetoxy-1-(4-methoxyphenyl)-4-phenyl-2-azetidinone, cis-(3R,4S)-3-

Rh soaked in polyionic gel: An effective catalyst for dehydrogenative silylation of ketones

(Chemical Equation Presented) A polyionic gel-soaked Rh catalyst allows the formation of synthetically useful diphenylsilyl (DPS) enols under mild conditions. The reaction proceeds through dehydrogenative silylation of ketones, affording the kinetic silyl

Allylpalladium umpolung in the three-component coupling synthesis of homoallylic amines

(Chemical Equation Presented) Homoallylic amines and α-amino esters were prepared via a Pd(II)-catalyzed coupling of boronic acids and 1,2-nonadiene with ethyl iminoacetate or aliphatic, aromatic, and heteroaromatic imines. The allylpalladium umpolung was

New methods for the synthesis of imidazoline-N-oxides

Δ3-imidazoline-3-oxides were prepared by the reaction of corresponding aromatic Schiff bases with syn-2-bromoacetophenone oxime. 5,6-Dihydro-4H-1,2,5-oxadiazines were isolated as byproduct in some instances.