260352-52-1

Upstream product

• 2627-86-3 (S)-1-phenyl-ethylamine 
• 612-23-7 2-nitrobenzyl chloride 
• 552-89-6 2-nitro-benzaldehyde 

Downstream Products

• 260352-54-3 (E)-But-2-enoic acid (2-nitro-benzyl)-((S)-1-phenyl-ethyl)-amide 
• 260352-55-4 N-(2-nitro-benzyl)-3-phenyl-N-(1-phenyl-ethyl)-acrylamide 
• 260352-53-2 N-(2-nitro-benzyl)-N-(1-phenyl-ethyl)-acrylamide 
• 918476-43-4 (S,S)-N,N'-bis-(2-nitrobenzyl) N,N'-bis-(1-phenylethyl)-oxalamide 
• 260352-61-2 C₂₇H₂₆ClN₃O₃ 
• 260352-60-1 C₂₂H₂₄ClN₃O₃ 
• 260352-59-8 C₂₁H₂₂ClN₃O₃ 
• 260352-58-7 N-(2-amino-benzyl)-3-phenyl-N-(1-phenyl-ethyl)-acrylamide 
• 260352-57-6 2-[N-(1-(S)-phenylethyl)-N-(1-oxo-2-(E)-butenyl)aminomethyl]aniline 
• 260352-56-5 N-(2-amino-benzyl)-N-(1-phenyl-ethyl)-acrylamide 

Relevant academic research and scientific papers

Facile synthesis of (S,S)-1,2-diacylamides and (S,S)-1,2-diamines with C2-symmetry

A series of chiral vicinal tertiary diacylamides with C2- symmetry was synthesized from (S)-α-phenylethylamine, different aromatic aldehydes, and oxalyl chloride. The diacylamides obtained were then reduced to afford chiral vicinal diamines wit

Asymmetric induction by the (S)-1-phenylethyl group in intramolecular nitrile imine cycloadditions giving enantiopure 3,3a-dihydro-pyrazolo[1,5- a][1,4]benzodiazepine-4(6H)-ones

Stereoselective intramolecular cycloadditions of homochiral nitrile imines 5 are described as a fruitful source of enantiopure 3,3a-dihydro- pyrazolo[1,5-a][1,4]benzodiazepine-4(6H)-ones 6 and 7. (C) 1999 Elsevier Science Ltd.