28504-96-3

Upstream product

• 26597-63-7 3-hydroxy-2-methyl-3-phenyl-2,3-dihydro-isoindol-1-one 
• 60-29-7 diethyl ether 
• 108-86-1 bromobenzene 
• 550-44-7 N-methylphthalimide 
• 591-51-5 phenyllithium 

Downstream Products

• 1265964-70-2 2-methyl-1-(4-methylphenyl)-3-phenyisoindole 
• 1265964-71-3 1-(4-methoxyphenyl)-2-methyl-3-phenylisoindole 
• 1265964-72-4 1-(4-trifluoromethylphenyl)-2-methyl-3-phenylisoindole 
• 1265964-73-5 2-methyl-1-(2-methylphenyl)-3-phenylisoindole 
• 1265964-74-6 2-methyl-1-phenyl-3-(3-pyridyl)isoindole 
• 1265964-79-1 5,12-dihydro-13-methyl-5,12-diphenylnaphthacene-5,12-imine 
• 4276-24-8 1,3-diphenyl-2-methylisoindole 
• 51802-87-0 2-methyl-1-phenyl-isoindole 

Relevant academic research and scientific papers

Integrated catalytic C-H transformations for one-pot synthesis of 1-arylisoindoles from isoindolines via palladium-catalyzed dehydrogenation followed by C-H arylation

A one-pot conversion of isoindolines to 1-arylisoindoles was established from palladium-catalyzed cascade C-H transformations, that is, the dehydrogenation of isoindolines to give isoindoles, with subsequent C-H arylation of the isoindoles.(Figure Presented)

Generation, Detection, and Reaction of Ammonium Ylides in Reactions of phenylcarbenes

Generation of diphenylcarbene (DPC) bearing a 2-(N,N-dimethylamino)methyl group in CHCl3 produced (N,N-dimethylamino)phenylisoindolium chloride and dichlorocarbene, which was trapped by added cyclohexene, while DPC having a 2-(N,N-dimethylamino)ethyl grou

Rearrangement of cis- and trans-2-Methyl-1-(substituted phenyl)isoindolinium 2-Methylides

Fluoride ion induced desilylation of cis-2-methyl-1-(substituted phenyl)-2-isoindolinium iodides cis-5 gave mixtures of the Sommelet-Hauser rearrangement products 7 and the Stevens products 8 in a ratio about 8.5:1.5.Similar treatments of the trans-isomer (trans-5) afforded exclusively 8.The pathways of the ylide rearrangement are discussed.