88459-86-3

Upstream product

• 1817-57-8 4-phenyl-3-butyne-2-one 
• 28164-29-6 4-phenylbut-3-yn-2-one oxime 
• 858641-30-2 dimethyl-tellurocarbamic acid Te-(3-oxo-1-phenyl-but-1-enyl) ester 
• 106011-93-2 bis(N,N-dimethylcarbamoyl) ditelluride 
• 255390-22-8 C₁₇H₁₅NO₃S 
• 936924-43-5 C₁₀H₉NOTe 

Downstream Products

• 1199525-57-9 C₂₀H₁₇NO 
• 1199525-71-7 C₂₅H₂₁NO₂S 
• 1199525-63-7 C₂₆H₁₉NO₂ 
• 1199525-65-9 C₂₅H₁₉NO 
• 1199525-52-4 C₁₆H₁₅NO₄ 
• 143806-23-9 4-phenyl-6-methylnicotinic acid methyl ester 
• 1199525-55-7 methyl 6-methyl-2,4-diphenylnicotinate 
• 1199525-60-4 C₁₇H₂₁NOSi 
• 1199525-69-3 C₁₅H₁₆N₂O 
• 1199525-56-8 C₁₈H₂₁NO₂ 
• 1199525-66-0 C₁₉H₁₅NO 

Relevant academic research and scientific papers

A convenient synthesis of isotellurazoles via deoxygenation of isotellurazole Te-oxide oligomers by using a combination of Ph3P/I2

Ynones and ynals bearing a variety of substituent were converted into isotellurazole Te-oxide oligomers through a convenient procedure via formation and ring closure of β-(N,N-dimethylcarbamoyltellurenyl)alkenyl ketones or aldehydes, and the subsequent co

Synthesis of isochalcogenazole rings by treating β-(N,N- dimethylcarbamoylchalcogenenyl)alkenyl ketones with hydroxylamine-O-sulfonic acid

β-(N,N-Dimethylcarbamoylselenenyl)- and β-(N,N- dimethylcarbamoyltellurenyl)alkenyl ketones were converted into isoselenazoles and isotellurazole Te-oxides, respectively, simply by treating with hydroxylamine-O-sulfonic acid, and deoxygenation of the latt