36029-70-6

Upstream product

• 696-62-8 para-iodoanisole 
• 321917-64-0 3,3,3-trifluoro-1,1-diphenyl-2-phenylsulfonylpropene 
• 108-86-1 bromobenzene 
• 1254220-97-7 C₂₂H₂₄BF₃O₃ 
• 13139-86-1 4-methoxyphenyl magnesium bromide 
• 36087-08-8 α-(Chlordifluormethyl)-α-(trifluormethyl)-p-methoxy-benzylalkohol 
• 36029-83-1 α-(Chlordifluormethyl)-α-(trifluormethyl)-p-methoxybenzylchlorid 
• 321917-62-8 3,3,3-trifluoro-1-phenyl-1-phenylsulfonyl-2-phenylthiopropene 
• 321917-63-9 3,3,3-trifluoro-1,1-diphenyl-2-phenylthiopropene 
• 321917-61-7 2,3,3,3-tetrafluoro-1-phenyl-1-phenylsulfonylpropene 
• 321917-60-6 2,3,3,3-tetrafluoro-1-phenyl-1-phenylthiopropene 
• 137504-63-3 2,2,3,3,3-pentafluoro-1,1-bis(phenylthio)propylbenzene 
• 591-51-5 phenyllithium 
• 1979-53-9 1-methoxy-4-(perfluoroprop-1-en-2-yl)benzene 

Downstream Products

• 52033-66-6 2-(4-methoxyphenyl)-3-phenyl-1H-indene 

Relevant academic research and scientific papers

Niobium-catalyzed activation of CF3 group on alkene: Synthesis of substituted indenes

A CF3 group attached to an alkene functionality was activated by a zero-valent niobium catalyst to generate niobium alkenylcarbenoid species. The niobium carbenoid species then underwent insertion to an internal aromatic C-H σ bond to give inde

Preparation of α- or β-trifluoromethylated vinylstannanes and their cross-coupling reactions

α - or β-Trifluoromethylated vinylstannanes 1, 2a, 3 and 4 were prepared form 1,1-bis(phenylthio)-2,2,3,3,3-pentafluoropropylbenzene (5) via several steps. The cross-coupling arylation reactions of 1-4 with aryl iodides bearing a bromo, methoxy, methyl, n