577749-34-9

Upstream product

• 577749-27-0 1-[2,6-di-t-butyldiphenylsilyloxy-(2S,4E)-4-hexenylsulfinyl]benzene 
• 108-98-5 thiophenol 
• 272776-88-2 1-(4-methoxybenzyloxy)-4-[(2S)-oxiran-2-yl]-2-butyne 
• 577749-32-7 6-phenylsulfanyl-(E,2S)-2-hexene-1,5-diol 
• 577749-31-6 6-phenylsulfanyl-(5S)-2-hexyne-1,5-diol 
• 577749-28-1 2-[4-(4-methoxy-benzyloxy)-but-2-ynyl]-oxirane 
• 577749-30-5 5-(4-methoxybenzyloxy)-1-phenylsulfanylmethyl-(1S)-3-pentynyl alcohol 
• 577749-33-8 1-[2,6-di-t-butyldiphenylsilyloxy-(2S,4E)-4-hexenylsulfanyl]benzene 

Downstream Products

• 1431543-10-0 C₅₁H₅₇BrO₅SSi₂ 
• 1431543-11-1 C₅₁H₅₇BrO₅SSi₂ 
• 1431543-06-4 C₄₆H₅₇BrO₅SSi₂ 
• 1431543-07-5 C₄₆H₅₇BrO₅SSi₂ 
• 577749-37-2 5-bromo-6-t-butyldiphenylsilyloxy-1-phenylsulfonyl-(2S,4R,5S)-hexane-2,4-diol 
• 577749-36-1 1-[1-bromo-2-hydroxy-(1S)-ethyl]-3-hydroxy-4-phenylsulfonyl-(1R,3S)-butyl alcohol 
• 577749-35-0 (2S,3R,5S)-6-Benzenesulfonyl-2-bromo-1,5-bis-(tert-butyl-diphenyl-silanyloxy)-hexan-3-ol 
• 577749-42-9 (2S,3R,5S)-6-Benzenesulfinyl-2-bromo-5-(tert-butyl-diphenyl-silanyloxy)-hexane-1,3-diol 

Relevant academic research and scientific papers

The sulfinyl moiety as an internal nucleophile. 2. Stereoselective synthesis of (-)-galantinic acid via 1,3-asymmetric induction

A stereoselective synthesis of (-)-galantinic acid is disclosed. The key steps include hydrolytic kinetic resolution of a racemic epoxide and regio- and stereoselective heterofunctionalization of an olefin, using a pendant sulfinyl group as the nucleophil