219141-86-3

Upstream product

• 71899-72-4 (2S,R_S)-1-(p-tolylsulfinyl)butan-2-ol 
• 219141-84-1 1-((R)-(R)-2-Azido-butane-1-sulfinyl)-4-methyl-benzene 

Downstream Products

• 219141-88-5 N-(1-p-tolylsulfanylmethyl-propyl)-benzamide 
• 219141-87-4 N-[(R)-1-((R)-Toluene-4-sulfinylmethyl)-propyl]-benzamide 

Relevant academic research and scientific papers

Stereoselective Synthesis of Enantiopure Amino Compounds, via Mitsunobu Azidation of (2S,Rs)-1-(p-Tolylsulfinyl)butan-2-ol

Azidation of (2S,Rs)-1-(p-tolysulfinyl)butan-2-ol under Mitsunobu conditions is the key step for a highly stereoselective preparation of enantiomerically pure amino compounds via chiral sulfoxide chemistry.