217947-27-8

Upstream product

• 49557-76-8 N-(4-methoxybenzylidene)benzenesulfonamide 
• 106-95-6 allyl bromide 
• 664985-99-3 (E)-N-(4-methoxybenzylidene)benzenesulfonamide 
• 98-10-2 benzenesulfonamide 
• 24165-60-4 1-(4-methoxyphenyl)but-3-en-1-ol 

Downstream Products

• 97974-64-6 1-(4-methoxyphenyl)but-3-en-1-amine 

Relevant academic research and scientific papers

Organometallic reactions in aqueous media. Indium-mediated allylation of sulfonimines

Barbier-type allylation of sulfonimines with indium and allyl bromide to give homoallylic sulfonamides can be performed smoothly in organic solvents and in aqueous media. The regio- and the stereoselectivity of the reaction have been examined.

Molybdenum(V) chloride-catalyzed amidation of secondary benzyl alcohols with sulfonamides and carbamates

A general and selective method for the direct amidation of secondary benzyl alcohols with both sulfonamides and carbamates is described. This method has been applied to a variety of substrates and the reaction proceeded smoothly at room temperature in the

Organometallic reactions in aqueous media. Indium- and zinc-mediated allylation of sulfonimines

Sulfonimines derived from aryl and nonenolizable aliphatic aldehydes can be effectively allylated to the corresponding homoallylic sulfonamides with allylic bromides promoted by indium or zinc. The solvent used can be water, THF, or a mixed aqueous THF solvent. The regioselectivity and stereoselectivity of the reaction were studied.