84363-65-5

Upstream product

• 84363-62-2 2-(phenylsulfonyl)-2-chloro-1-(trimethylsilyl)octane 
• 60012-73-9 Phenylsulfonyl-2-octanol-1 
• 73476-18-3 1-benzenesulfonyl-2-trimethylsilylethane 
• 629-05-0 n-octyne 
• 80-17-1 benzenesufonyl hydrazide 
• 638-45-9 1-Iodohexane 
• 108-98-5 thiophenol 
• 20611-21-6 2-(phenylsulfonyl)ethanol 
• 699-12-7 2-(phenylthio)ethanol 
• 84363-56-4 2-(phenylsulfonyl)-1-(trimethylsilyl)octane 
• 84363-73-5 1-acetyl-1-(phenylsulfonyl)-2-(trimethylsilyl)ethane 
• 84363-72-4 3-benzenesulfonyl-4-trimethylsilyl-2-butanol 
• 84363-74-6 1-(phenylsulfonyl)-1-chloro-2-(trimethylsilyl)ethane 

Downstream Products

• 28665-60-3 (E)-1-phenyl-1-octene 

Relevant academic research and scientific papers

Direct transformation of terminal alkynes to branched allylic sulfones

A new strategy for the transformation of terminal alkynes to branched allylic sulfones was developed. Using a Rh(I)/DPEphos/benzoic acid catalyst system, terminal alkynes react with sulfonyl hydrazides to produce branched allylic sulfones with good to exc

Facile synthesis of vinyl sulfones from β-bromo alcohols

Vinyl sulfones are synthesized in good yields by dehydration of β- hydroxy sulfones derived from β-bromo alcohols.

1-BENZENESULFONYL-2-TRIMETHYLSILYLETHANE AND 1-BENZENESULFONYL-1-CHLORO-2-TRIMETHYLSILYLETHANE; EFFICIENT REAGENTS FOR SULFONYL-α-VINYLATION

1-Benzenesulfonyl-2-trimethylsilylethane and 1-benzenesulfonyl-1-chloro-2-trimethylsilylethane are convertable to 1-benzenesulfonyl-1-chloro-1-substituted-2-trimethylsilylethanes which undergo elimination by fluoride ion to give phenyl α-substituted-vinyl