445235-51-8

Upstream product

• 98-83-9 isopropenylbenzene 
• 6006-81-1 3-hydroxy-2-phenylpropene 
• 5155-87-3 3-phenylbut-3-enoic acid 
• 127-65-1 chloroamine-T 

Downstream Products

• 497172-43-7 dimethyl 2-(2-phenyl-2-propenyl)-2-(2-propynyl)malonate 
• 58567-50-3 N-[2-(phenyl)prop-2-en-1-yl]-N-(p-toluenesulfonyl)amide 
• 5155-87-3 3-phenylbut-3-enoic acid 
• 1402160-62-6 C₁₇H₁₄O₂ 
• 1402160-47-7 C₁₇H₁₄O₂ 
• 1374602-53-5 3-(methoxycarbonyl)-3-(2-phenylallyl)-5-butyl-2(3H)-furanone 
• 1374602-57-9 3-(methoxycarbonyl)-3-(2-phenylallyl)-5-phenyl-2(3H)-furanone 
• 117794-76-0 N-prop-2-yn-1-yl-N-[2-(phenyl)prop-2-en-1-yl]-N-(p-toluenesulfonyl)amide 

Relevant academic research and scientific papers

Iodine-Catalyzed Decarboxylative Amidation of β,γ-Unsaturated Carboxylic Acids with Chloramine Salts Leading to Allylic Amides

The iodine-catalyzed decarboxylative amidation of β,γ-unsaturated carboxylic acids with chloramine salts is described. This method enables the regioselective synthesis of allylic amides from various types of β,γ-unsaturated carboxylic acids containing sub

Electrophilic monoiodination of terminal alkenes

An excess of elemental iodine in N,N-dimethylacetamide enables effective 3/iodanylium-de-hydronation of terminal alkenes with 3-iodopropene derivatives and hydrogen iodide formation within minutes at room temperature. The optimal molar ratio of iodine to

Investigation of intramolecular Pauson-Khand reaction of 2-aryl-1,6- and 1-methyl-1,7-enynes (exo-olefins) and 1-phenyl-1-octen-7-yne (endoolefin)

The intramolecular Pauson-Khand reaction of various 2-aryl-1-hepten-6-ynes and its aza-derivatives (exo-olefins) efficiently produced arylbicyclo[3.3.0]octenones and azaoctenone bearing quaternary carbon centers at angular positions in good yields. Although a similar reaction of 2-phenyl-1-octen-7-yne (exo-olefin), which is a homologue of 2-phenyl-1-hepten-6-yne, did not take place, the reaction of the methyl derivatives smoothly proceeded. However, the reaction of regioisomeric 1-phenyl-1-octen-7-yne (endo-olefin) afforded the desired product in moderate yields.

An intriguing effect of Yb(OTf)3-TMSCl in the halogenation of 1,1-disubstituted alkenes by NXS: Selective synthesis of allyl halides

A novel protocol to effect the efficient selective halogenation of 1,1-disubstituted alkenes with NXS catalyzed by Yb(OTf)3-TMSCl, which affords the corresponding allyl halides in high yield, including allyl bromide, chloride, iodide and fluori