80396-17-4

Upstream product

• 1083-30-3 dihydrochalcone 
• 120238-42-8 methyl (S)-2-(diphenylmethylideneamino)-3-phenylpropanoate 
• 131472-77-0 2-(Benzhydrylidene-amino)-1,3-diphenyl-propan-1-ol 
• 120-46-7 1,3-diphenylpropanedione 
• 614-47-1 1,3-diphenyl-propen-3-one 
• 55181-05-0 ω-phenyl isonitrosopropiophenone 
• 18315-79-2 E-β-benzoyl-β-nitrostyrene 
• 51210-89-0 1,3-diphenyl-2-oximino-1,3-propanedione 

Downstream Products

• 861055-73-4 dichloro-acetic acid-[1-(α-hydroxy-benzyl)-2-phenyl-ethylamide] 
• 78631-09-1 acetamido-2 diphenyl-1,3 propanol-1 
• 78631-05-7 cis-benzyl-4 methyl-2 phenyl-5 oxazoline-2 chlorhydrate 
• 1429616-35-2 4-acetyl-N-(1-phenyl-2,3-dihydro-1H-inden-2-yl)benzamide 

Relevant academic research and scientific papers

Acid controlled generation of indanes and oxazolines from β-hydroxyarylethanamide

Simple and efficient protocols for the construction of substituted indanes and oxazolines through intramolecular cyclization of β- hydroxyarylethanamide using trifluoromethanesulfonic acid and titanium tetrachloride in 1,2-dichloroethane respectively have

β-Amino alcohols from amino acids: Chelation control via Schiff bases

Sequential addition of iBu2AlH and RLi or RMgX to Schiff base esters derived from amino acids provides a simple route to β-amino alcohols. The reaction procedes without racemization, and with high threo selectivity. Several representative sphingosines are synthesized.

Preparation, reduction chimique et electrochimique d'α-nitrostyrylcetones - synthese d'heterocycles azotes

Nitration of styryl ketones with nitrogen peroxide leads to the corresponding α-nitroethylenic ketones in good yield.However, the presence of methoxy groups involves a nitration on the aromatic nucleus.LiAlH4 reduction of α-nitrostyrylketones yields the c