65885-20-3

Upstream product

• 16212-06-9 phenyl styryl sulfone 
• 124-40-3 dimethyl amine 
• 20599-29-5 (α-butoxy-benzyl)-dimethyl-amine 
• 85608-10-2 C₇H₇ClMgO₂S 
• 3112-85-4 methylphenylsulfonate 
• 536-74-3 phenylacetylene 
• 108-98-5 thiophenol 
• 5418-11-1 phenyl styryl sulfone 

Downstream Products

• 72568-90-2 (E)-((1-phenylprop-1-en-2-yl)sulfonyl)benzene 
• 30246-74-3 {[(1E)-1-phenylprop-1-en-2-yl]sulfonyl}benzene 
• 75032-59-6 ((1R,2R)-2-Benzenesulfonyl-1-phenyl-propyl)-dimethyl-amine 
• 75032-56-3 ((1S,2R)-2-Benzenesulfonyl-1-phenyl-propyl)-dimethyl-amine 

Relevant academic research and scientific papers

Action d'organometalliques fonctionnels sur des gem-aminoethers et des sels d'immonium. I. Synthese d'amines α- ou β-fonctionnelles difficilement accessibles par reaction de Mannich

Some α- or β-functional amines which are difficult to obtain by Mannich reaction can be easily prepared from organomagnesium or organozinc functional derivatives and gem-aminoethers or immonium salts.

Directed Diastereotopic Lithiation of β-Heterosubstituted Alkyl Sulfones

The directed, highly diastereoselective lithiation of β-aminoalkyl sulfones by organolithium reagents has been shown capable of producing either diastereomeric lithio derivative with greater than 90percent selectivity, depending upon the type of amino group.