39219-48-2

Upstream product

• 6597-75-7 1-(4-acetamidophenoxy)-2,3-epoxypropane 

Downstream Products

• 125452-50-8 (S)-6-[(R)-3-(4-Acetylamino-phenoxy)-2-hydroxy-propylamino]-heptanoic acid (4-trifluoromethyl-phenyl)-amide 
• 125452-48-4 (R)-6-[(R)-3-(4-Acetylamino-phenoxy)-2-hydroxy-propylamino]-heptanoic acid (4-trifluoromethyl-phenyl)-amide 
• 37936-66-6 (+)-Practolol 

Relevant academic research and scientific papers

Enantioselective ring opening of epoxides with trimethylsilyl azide (TMSN3) in the presence of β-cyclodextrin: An efficient route to 1,2-azido alcohols

The ring opening of epoxides with nucleophiles such as TMSN3 and isopropylamine takes place enantioselectively in the presence of β- cyclodextrin under extremely mild conditions and the azido alcohols and amino alcohols are formed as (S)-isomers. (C) 1999 Published by Elsevier Science Ltd.