40339-47-7

Upstream product

• 123-11-5 4-methoxy-benzaldehyde 
• 62-53-3 aniline 

Downstream Products

• 57427-78-8 (4Z)-4-(4-methoxybenzylidene)-2-phenyl-oxazolin-5-one 
• 101067-83-8 (3R,4S)-4-(4-Methoxy-phenyl)-1,3-diphenyl-3-trimethylsilanyloxy-azetidin-2-one 
• 93681-35-7 (Z)-3-[(2R,3S)-2-(4-Methoxy-phenyl)-4-oxo-1-phenyl-azetidin-3-ylamino]-but-2-enoic acid methyl ester 
• 57880-71-4 3,3-dichloro-4-(p-methoxyphenyl)-1-phenyl-2-azetidinone 
• 101067-86-1 (3R,4S)-3-Hydroxy-4-(4-methoxy-phenyl)-1,3-diphenyl-azetidin-2-one 
• 7380-78-1 4-(phenylethynyl)anisole 
• 182824-73-3 (3R,4S)-4-(4-Benzyloxy-phenyl)-3-[(S)-2-(4-fluoro-phenoxy)-1-hydroxy-ethyl]-1-(4-fluoro-phenyl)-azetidin-2-one 

Relevant academic research and scientific papers

Unlocking the catalytic potential of tris(3,4,5-trifluorophenyl)borane with microwave irradiation

The catalytic activity of tris(3,4,5-trifluorophenyl)borane has been explored in the 1,2-hydroboration reactions of unsaturated substrates. Under conventional conditions, the borane was found to be active only in the hydroboration of aldehyde, ketone and imine substrates, with alkenes and alkynes not being reduced effectively. The use of microwave irradiation on the other hand has permitted alkenes and alkynes to be hydroborated in good yields.

Synthesis of 3-benzylxanthine and lumazine analogues

Several xanthines (7-13) are prepared by the cyclisation of 1-benzyl-5,6-diaminouracil with single-carbon inserting agents such as aromatic aldehydes, formamides, acetic anhydride, carbon disulfide, and nitrous acid. Treatment of 6-amino-1-benzyl-5-nitros

Poly(ethylene glycol) supported liquid-phase synthesis of 1,2,4-oxadiazolines

The liquid-phase synthesis of oxadiazolines via 1,3-dipolar cycloaddition reaction on poly(ethylene glycol) support (PEG) is described. 1,3-Dipolar cycloadditions of nitrile oxide generated in situ on soluble polymer with a variety of imines provided a li

Synthesis of C3 heteroatom-substituted azetidinones that display potent cholesterol absorption inhibitory activity

The C3 phenylpropyl side chain N-phenylazetidinones related to SCH 56524 was modified by replacing the hydroxymethylene with various isoelectronic or isosteric groups. Modifications at the 3' position led to less-active compounds; however, modifications a