56161-48-9

Upstream product

• 107-21-1 ethylene glycol 
• 108-98-5 thiophenol 
• 107-02-8 acrolein 
• 18742-02-4 2-bromo-2-(2-ethyl)dioxolane 
• 1212-08-4 S-Phenyl benzenethiosulfonate 

Downstream Products

• 117626-71-8 (+/-)-2-<2-chloro-2-(phenylthio)ethyl>-1,3-dioxolane 
• 105621-12-3 2-((Z)-2-Phenylsulfanyl-vinyl)-[1,3]dioxolane 
• 105621-12-3 (E)-2-<2-(phenylthio)ethenyl>-1,3-dioxolane 
• 56161-51-4 2-<2-(phenylsulfonyl)ethyl>-1,3-dioxolane 
• 117626-60-5 2-exo,3-exo-diethenyl-4-methyl-5-(phenylthio)-7-oxabicyclo<2.2.1>heptane 
• 117626-74-1 (1R,2S,3R,4R,5R)-4-Methyl-5-phenylsulfanyl-3-vinyl-7-oxa-bicyclo[2.2.1]heptane-2-carbaldehyde 
• 117626-72-9 (+/-)-(E)-4-(1,3-dioxolan-2-yl)-3-(phenylthio)-3-buten-2-ol 
• 117626-59-2 3-exo-ethenyl-4-methyl-5-endo-(phenylthio)-7-oxabicyclo<2.2.1>heptane-2-exo-methanol 
• 117707-08-1 4-methyl-5-endo-(phenylthio)-7-oxabicyclo<2.2.1>heptane-2-exo,3-exo-dimethanol 
• 117626-67-2 1-methyl-2,3-bis(methylene)-5-exo-methoxy-5-endo-(phenylthio)-6-exo-chloro-7-oxabicyclo<2.2.1>heptane 
• 117626-64-9 4-methyl-5-(phenylthio)-7-oxabicyclo<2.2.1>hept-5-ene-2-exo,3-exo-dimethanol 
• 117626-57-0 (1S,2S,6R,7S,9S)-1-Methyl-9-phenylsulfanyl-4,10-dioxa-tricyclo[5.2.1.0^2,6]decane-3,5-dione 
• 117626-65-0 1-methyl-5-exo-methoxy-5-endo-(phenylthio)-6-exo-chloro-7-oxabicyclo<2.2.1>heptane-2-exo,3-exo-dimethanol 
• 117707-10-5 [(1S,2S,3R,4S,5S)-3-(tert-Butyl-dimethyl-silanyloxymethyl)-4-methyl-5-phenylsulfanyl-7-oxa-bicyclo[2.2.1]hept-2-yl]-methanol 

Relevant academic research and scientific papers

Electroreductive Nickel-Catalyzed Thiolation: Efficient Cross-Electrophile Coupling for C?S Formation

Sulfur-containing molecules are of utmost topical importance towards the effective development of pharmaceuticals and functional materials. Herein, we present an efficient and mild electrochemical thiolation by cross-electrophile coupling of alkyl bromide

A FACILE ELABORATION OF ALDEHYDES TO 2-ALKYL-3-THIOPHENYLFURANS

A two-step procedure for the elaboration of aldehydes to 2-substituted 3-thiofurans has been developed.The key step involves a site-selective deprotonation of a substituted vinyl sulfide.