64790-77-8

Upstream product

• 2396-68-1 4-t-butylbenzenethiol 

Downstream Products

• 128729-16-8 N-(4-t-Butylphenylsulfinyl)-3,5-di-t-butylaniline 
• 1264737-54-3 N-(4-methylbenzenesulfonyl) 4-tert-butylphenyl sulfonimidoyl fluoride 
• 1264737-69-0 N-(4-tert-butylbenzenesulphonyl)-4-methylbenzene-trifluoromethyl sulfoximine 
• 1264737-49-6 N-(4-methylbenzenesulfonyl) 4-tert-butylphenyl sulfonimidoyl chloride 
• 1027898-36-7 C₁₇H₁₈Cl₂N₂O₂S 
• 187342-34-3 C₁₇H₁₉ClN₂O₂S 

Relevant academic research and scientific papers

Regio- and Stereoselective Chloro Sulfoximidations of Terminal Aryl Alkynes Enabled by Copper Catalysis and Visible Light

By visible-light photoredox catalysis with copper complexes, sulfoximidoyl chlorides add to terminal aryl alkynes to give the corresponding (E)-β-chlorovinyl sulfoximines with exclusive regio- and stereoselectivities in high yields. Two representative pro

Synthesis of CF3-substituted sulfoximines from sulfonimidoyl fluorides

N-Protected trifluoromethyl-substituted sulfoximines have been prepared by treatment of sulfonimidoyl fluorides with a combination of the Ruppert-Prakash reagent (TMSCF3) and tetrabutyl ammonium fluoride (TBAF). The starting materials were accessed following two synthetic routes, and for each reaction sequence the substrate scope was evaluated. Accordingly, a wide variety of aryl-substituted products were obtained in moderate to good yield.