874209-67-3

Upstream product

• 874209-65-1 (S)-2-(1-Ethyl-1-methoxy-propyl)-1-((R)-1-phenyl-ethyl)-aziridine 
• 64-19-7 acetic acid 
• 397849-98-8 N-[(R)-(+)-α-methylbenzyl]aziridine-2-(S)-carboxylic acid menthyl ester 

Downstream Products

• 874209-69-5 (S)-3-Ethyl-3-methoxy-2-((R)-1-phenyl-ethylamino)-pentan-1-ol 

Relevant academic research and scientific papers

Synthesis of sterically controlled chiral β-amino alcohols and their application to the catalytic asymmetric sulfoxidation of sulfides

Sterically hindered and enantiomerically pure β-amino alcohols 8a and 8b were prepared from the enantiomerically pure aziridine-2-carboxylic acid menthol ester 13. Vanadium complexes of the chiral Schiff-base ligands prepared from the β-amino alcohols catalyze an efficient enantioselective sulfoxidation of alkyl aryl sulfides, while enantioselectivities as high as 96% ee can be observed in the sulfoxidation of benzyl aryl sulfides.