956215-93-3

Upstream product

• 4224-87-7 4-methyl-chalcone 
• 27126-76-7 [hydroxy(tosyloxy)iodo]benzene 

Downstream Products

• 2430-99-1 1-phenyl-2-p-tolylethanone 
• 74007-52-6 3,3-Dimethoxy-1-phenyl-2-p-tolyl-propan-1-one 
• 1202019-61-1 4-(4-methylphenyl)-5-phenylpyrazole-1-carboxamide 
• 1202019-66-6 4-(4-methylphenyl)-5-phenylpyrazole-1-thiocarboxamide 
• 116485-66-6 C₁₆H₁₃NO 

Relevant academic research and scientific papers

The chemistry of α,β-ditosyloxy ketones: A new and convenient route to 4,5-diarylisoxazoles from α,β-chalcone ditosylates

The reaction of α,β-chalcone ditosylates with hydroxyl-amine hydrochloride under suitable conditions leads to a 1,2-aryl shift, thereby providing a new route to 4,5-disubstituted isoxazoles. Georg Thieme Verlag Stuttgart. New York.

The chemistry of α,β-ditosyloxyketones: new and convenient route for the synthesis of 1,4,5-trisubstituted pyrazoles from α,β-chalcone ditosylates

The reaction of α,β-chalcone ditosylates with various reagents such as phenylhydrazine hydrochloride, semicarbazide hydrochloride and thiosemicarbazide in suitable conditions leads to 1,2-aryl shift, thereby providing a novel route for the synthesis of 1,4,5-trisubstituted pyrazoles.

The chemistry of α,β-ditosyloxyketones: Novel routes for the synthesis of desoxybenzoins and α-aryl-β-ketoaldehyde dimethylacetals from α,β-chalcone ditosylates

The reaction of α,β-chalcone ditosylates 3 with potassium hydroxide in suitable conditions leads to 1,2-aryl shift and carbon-carbon bond cleavage, thereby providing a novel route for the synthesis of 1,2-diarylethan-1-ones 4 and 1,2-diaryl-3,3-dimethoxy propan-1-ones 5. Georg Thieme Verlag Stuttgart.