31616-26-9

Upstream product

• 3886-69-9 (R)-1-phenyl-ethyl-amine 
• 95-92-1 oxalic acid diethyl ester 
• 79-37-8 oxalyl dichloride 

Downstream Products

• 76740-22-2 (+)-N,N'-Bis<(R)-1-phenylethyl>-1,2-ethylendiamin 

Relevant academic research and scientific papers

Resolution of α-phenylethylamine by its acidic derivatives

α-Phenylethylamine was resolved by its own derivatives formed with a homologous series of dicarboxylic acids. The structure of the oxalamic acid diastereoisomeric salts was investigated by the single-crystal X-ray diffraction method.

Chiral phosphinamides: New catalysts for the asymmetric reduction of ketones by borane

We have identified a new class of catalysts for the asymmetric reduction of prochiral ketones by borane. Key to the architecture of effective catalysts is an N-P=O structural unit which may be part of a phosphinamide, phosphonamide or a related structure.