1412945-24-4

Upstream product

• 1412945-23-3 2-{(2R,3R)-3-[(tert-butyldimethylsiloxy)methyl]oxiran-2-yl}ethanol 
• 98-59-9 p-toluenesulfonyl chloride 
• 146916-76-9 5-(4-methoxyphenyl)methoxy-2-pentyn-1-ol 
• 242808-65-7 ((2R,3R)-3-(2-(4-methoxybenzyloxy)ethyl)oxiran-2-yl)methanol 
• 1412945-22-2 (2R,3R)-2-[(tert-butyldimethylsiloxy)methyl]-3-[2-(4-Methoxybenzyloxy)ethyl]oxirane 
• 158817-21-1 (E)-5-(4-methoxybenzyloxy)pent-2-en-1-ol 

Relevant academic research and scientific papers

Asymmetric syntheses of all stereoisomers of 3-hydroxyproline; A constituent of several bioactive compounds

Synthesis of an unusual β-hydroxy-α-amino acid, 3-hydroxyproline, and its derivatives have been achieved enantioselectively by employing Sharpless asymmetric epoxidation and reductive cyclization as the key steps. Georg Thieme Verlag Stuttgart ? New York.