104515-61-9

Upstream product

• 87-17-2 salicylanilide 
• 106-95-6 allyl bromide 

Downstream Products

• 126255-54-7 3,4-dihydro-3-ethyl-1-phenyl-5H-benzopyrano<4,3-b>pyridin-2(1H)-one 
• 126219-00-9 C₂₁H₁₉NO₄ 
• 104515-47-1 2-Allyloxy-N-phenyl-thiobenzamide 
• 112794-49-7 2-(Allyloxy)-N¹,N²-diphenylbenzamidin 
• 112794-51-1 2-<2-(Allyloxy)phenyl>-3,6-dihydro-5-methyl-6-oxo-1,3-diphenyl-1-pyrimidinium-4-olat 
• 112794-57-7 8-Benzyl-10,11-diphenylbenzo-4-oxa-10,11-diazatricyclo<6.2.2.0^1,6>dodec-2-en-9,12-dion 
• 112794-55-5 2-<2-(Allyloxy)phenyl>-5-benzyl-3,6-dihydro-6-oxo-1,3-diphenyl-1-pyrimidinium-4-olat 
• 112794-50-0 8-Methyl-10,11-diphenylbenzo-4-oxo-10,11-diazatricyclo<6.2.2.0^1,6>dodec-2-en-9,12-dion 
• 104515-53-9 C₂₄H₁₉NO₂S 

Relevant academic research and scientific papers

Intramolecular 1,4-Dipolar Cycloadditions utilizing Heteroaromatic Betaines

anhydro-2-(2-Allyloxyphenyl)-3,5-diphenyl-4-hydroxy-6-oxo-1,3-thiazinium hydroxide and the corresponding ethynyl derivative underwent ready thermal 1,4-dipolar cycloaddition to give a 1:1-cycloadduct (whose structure was determined by X-ray crystallograph

Pyrolysis of O-Allyl Salicylic Amides and Esters, and Related Compounds: Foemation of Isoindolones and Phthalides

Flash vacuum pyrolysis of O-allyl salicylic alkylamides and alkyl esters gives isoindolones and phthalides, respectively, in low (20-40percent) yield.The mechanism involves generation of the phenoxyl radical, regiospecific hydrogen-atom transfer from the alkylamide (or alkyl ester) group and cyclization.A similar sequence was observed with thiophenoxyl radicals.

Carbon-Carbon Bond Formation via Intramolecular Cycloadditions: Use of the Thiocarbonyl Ylide Dipole in anhydro-4-Hydroxythiazolium Hydroxides

The mesoionic systems resulting from the introduction of 2-(allyloxy)phenyl substituents into the 2-, 3-, and 5-positions of anhydro-4-hydroxythiazolium hydroxide undergo intramolecular cycloaddition under different reaction conditions, the ease of cycloa