75854-97-6

Upstream product

• 104-93-8 p-methylanizole 
• 108-88-3 toluene 
• 4009-98-7 (methoxymethyl)triphenylphosphonium chloride 
• 1579999-77-1 1-(1-methoxyprop-1-en-2-yl)-3-methylbenzene 
• 78-94-4 methyl vinyl ketone 

Downstream Products

• 75855-01-5 4-(3-Dibromomethyl-phenyl)-4-methyl-cyclohexanone 
• 75855-02-6 (m-formylphenyl)-4 methyl-4 cyclohexene-2 one-1 
• 75855-00-4 4-Methyl-4-m-tolyl-cyclohexanone 

Relevant academic research and scientific papers

Asymmetric Induction at Remote Quaternary Centers of Cyclohexadienones by Rhodium-Catalyzed Conjugate Hydrosilylation

The enantioselective desymmetrizing conjugate hydrosilylation of prochiral differently γ,γ-disubstituted cyclohexadienone derivatives 2 to furnish the corresponding cyclohexenones 4 with a remote chiral all-carbon quaternary center at the γ position is de

Diprotonation de derives phenoliques. Nouvelle synthese d'aryl-4 et d'aryl-3 cyclohexenones et de benzobicycloheptanes.

In SbF5-HF paracresol and its methyl ether are diprotonated and react with monosubstituted benzenes (chlorobenzene, toluene, acetanilide) to give as primary products and after hydrolysis 4-aryl cyclohexenones 4, 7, 9.The higher the acidity, the faster is