89556-80-9

Upstream product

• 6361-21-3 2-chloro-5-nitrobenzaldehyde 
• 17480-69-2 (S)-N-benzyl-1-phenylethylamine 
• 100-52-7 benzaldehyde 
• 89556-73-0 (-)(S)-N-(α-methylbenzyl-N-benzylamine)sulfamide 
• 3129-98-4 (S)-N-benzylidene(1-phenylethylamine) 
• 2627-86-3 (S)-1-phenyl-ethylamine 
• 89556-76-3 (S)-N-(2-chloro-5-nitrobenzylidene)-N'-(α-methylbenzyl)-N'-benzylsulfamide 

Downstream Products

• 1517-74-4 (+)-(R)-isopropyl p-tolyl sulfoxide 

Relevant academic research and scientific papers

Chemistry of Oxaziridines. 8. Asymmetric Oxidation of Nonfunctionalized Sulfides to Sulfoxides with High Enantioselectivity by 2-Sulfamyloxaziridines. The Influence of the Oxaziridine C-Aryl Group on the Asymmetric Induction

Chiral sulfamyloxaziridines 6 and 7, prepared by biphasic oxidation of the corresponding sulfamylimines 5, afford high asymmetric induction for the oxidation of a series of nonfunctionalized sulfides to sulfoxides (53-91percent ee).The enantioselectivitie

Chiral Sulfamides: Synthesis of Optically Active 2-Sulfamyloxaziridines. High Enantioselectivity in the Asymmetric Oxidation of Sulfides to Sulfoxides

The first synthesis of optically active 2-sulfamyloxaziridines 4a-d and 5a-d, which affords high enantioselectivity (38-68 percent ee) for asymmetric oxidations of sulfides to sulfoxides, is described.