103660-94-2

Upstream product

• 100-52-7 benzaldehyde 
• 103660-91-9 (+)-(R)-p-tolyl sulphinyl-N,N-dimethylthioacetamide 
• 1517-82-4 (-)-(S)-menthyl toluene-p-sulphinate 

Relevant academic research and scientific papers

ASYMMETRIC SYNTHESIS OF β-HYDROXYTHIOACETAMIDES MEDIATED BY ENANTIOMERICALLY PURE SULPHINYL DERIVATIVES.

Enantiomerically pure p-tolyl sulphinyl-N,N-dimethylthioacetamide (1) was prepared starting from (-)-(S)-menthyl toluene-p-sulphinate.Aldol-type condensation of (1) and subsequent removal of the sulphinyl group open an entry to optically active β-hydroxy thioacetamides in 40-90percent e.e.