75910-47-3

Upstream product

• 110-89-4 piperidine 
• 59096-68-3 1-p-Chlorphenyl-3-p-toluolsulfonyl-propen-⁽²⁾-on-⁽¹⁾ 
• 75910-29-1 1-(4-chlorophenyl)-3-tosylpropan-1-one 
• 75-52-5 nitromethane 
• 99-91-2 para-chloroacetophenone 
• 75910-34-8 2-Bromo-1-(4-chloro-phenyl)-3-(toluene-4-sulfonyl)-propan-1-one 

Downstream Products

• 115809-11-5 6-(4-chlorophenyl)-2-thioxo-1,2-dihydropyridine-3-carbonitrile 

Relevant academic research and scientific papers

Electrosynthesis of enaminones directly from methyl ketones and amines with nitromethane as a carbon source

An efficient and mechanistically different method for the electrosynthesis of enaminone directly from methyl ketones, amines and nitromethane was developed. This transition-metal-free method proceeded at room temperature to give a wide array of enaminones

Reactions of &α,&β-Unsaturated &γ-Oxosulfones with Nucleophiles

Bromination of the γ-oxosulfones 1 and subsequent dehydrohalogenation leads to the α,β-unsaturated γ-oxosulfones 3.These products react with primary and secondary amines to yield the enaminoketones 7. γ-Oxobissulfones 10 are formed from 3 by addition of t