111533-89-2

Upstream product

• 108-98-5 thiophenol 
• 111506-75-3 (2R)-1-chloro-3-phenylsulphonylpropan-2-ol 
• 66536-75-2 (S)-(+)-1-(phenylsulfonyl)propan-2-ol 
• 22198-54-5 1-chloro-3-phenylsulfanylpropan-2-one 
• 23886-96-6 1-chloro-3-phenylsulphonylpropane-2-one 
• 111533-44-9 (2S,3S)-3-phenylsulphonylhept-5-en-2-ol 

Relevant academic research and scientific papers

Synthesis of Enantiomerically Pure 2,5-Disubstituted Teterahydrofurans Using Readily Prepared (2S)-1-Phenylsulphonylalkan-2-ols

Enantiomerically pure (2S)-1-phenylsulphonylalkan-2-ols have been prepared from 1-chloro-3-phenylsulphonylpropan-2-one (2) by the folloving successive procedures: reduction with baker's yeast, epoxidation with silver(I) oxide, and alkylation with