111506-77-5

Upstream product

• 15890-72-9 laurylmagnesium bromide 
• 105983-23-1 (2S)-1,2-epoxy-3-phenylsulphonylpropane 
• 23886-96-6 1-chloro-3-phenylsulphonylpropane-2-one 
• 22198-54-5 1-chloro-3-phenylsulfanylpropan-2-one 
• 111506-75-3 (2R)-1-chloro-3-phenylsulphonylpropan-2-ol 
• 108-98-5 thiophenol 
• 930-69-8 sodium thiophenolate 

Downstream Products

• 111533-84-7 (3S,5R,6S)-3,6-epoxy-5-phenylsulphonylnonadec-1-ene 
• 111533-83-6 (3R,5R,6S)-3,6-epoxy-5-phenylsulphonylnonadec-1-ene 
• 111533-68-7 (2S,3R)-3-Benzenesulfonyl-5-(1-phenylselanyl-ethyl)-2-tridecyl-tetrahydro-furan 
• 111533-56-3 (5R,6S)-5-phenylsulphonylnonadec-2-en-6-ol 
• 111533-56-3 (5S,6S)-5-phenylsulphonylnonadec-2-en-6-ol 

Relevant academic research and scientific papers

Synthesis of Enantiomerically Pure (4S)-2-Alken-4-olides via (2S)-1-Phenylsulfonyl-2-alkanols

Reduction of 1-chloro-3-phenylsulfonyl-2-propanone with baker's yeast, followed by epoxidation and alkylation with Grignard reagents, yields enantiomerically pure (2S)-2-phenylsulfonyl-2-alkanols, which are converted into (4S)-2-alken-4-olides in 100perce

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