648908-26-3

Upstream product

• 783-08-4 [4-(benzylideneamino)phenyl]methanol 

Downstream Products

• 648908-42-3 (2R,3R)-2-decyl-2-ethoxycarbonyl-1-(4-methoxyphenyl)-3-phenylaziridine 
• 648908-38-7 (2S,3R)-2-decyl-2-deuterio-1-(4-methoxyphenyl)-3-phenylaziridine 
• 648908-44-5 ethyl (S)-2-acetamino-2-benzyldodecanoate 
• 648908-31-0 (2S,3R)-2-decyl-2-methyl-1-(4-methoxyphenyl)-3-phenylaziridine 
• 648908-37-6 (2S,3R)-2-decyl-1-(4-methoxyphenyl)-3-phenylaziridine 
• 648908-43-4 ethyl (S)-2-amino-2-benzyldodecanoate 
• 648908-33-2 (S)-(+)-N-(1-benzyl-1-methylundecyl)acetamide 
• 648908-41-2 (S)-N-(1-benzyl-1-deuterioundecyl)acetamide 
• 648908-39-8 (S)-N-(1-benzylundecyl)acetamide 
• 648908-29-6 (2R,3R,R_S)-2-decyl-1-(4-methoxyphenyl)-3-phenyl-2-(p-tolylsulfinyl)aziridine 

Relevant academic research and scientific papers

A new synthesis of enantiomerically pure α- and β-amino acid derivatives using aziridinyl anions

Optically active sulfinylaziridines having a 4-methoxyphenyl group on their nitrogen atom were synthesized from optically active 1-chloroalkyl p-tolyl sulfoxide and an imine derived from benzaldehyde and p-anisidine stereoselectively in good overall yield