55023-86-4

Upstream product

• 65399-00-0 2,3-dihydro-2-(1-methylethyl)-1H-isoindol-1-one 
• 304-17-6 N-isopropylphthalimide 
• 117135-91-8 2-isopropylisoindoline 
• 117135-98-5 2-Isopropylisoindolin-N-oxid 

Downstream Products

• 123542-19-8 10-isopropyl-2-phenyl-3a,4,9,9a-tetrahydro-1H-4,9-epiminobenzo[f]isoindole-1,3(2H)-dione 
• 123542-21-2 endo-1,2,3,4-Tetrahydro-9-isopropyl-N-(4-methoxyphenyl)-1,4-iminonaphthalin-2,3-dicarboximid 
• 123620-17-7 exo-1,2,3,4-Tetrahydro-9-isopropyl-N-phenyl-1,4-iminonaphthalin-2,3-dicarboximid 
• 123620-18-8 exo-1,2,3,4-Tetrahydro-9-isopropyl-N-(4-methylphenyl)-1,4-iminonaphthalin-2,3-dicarboximid 
• 123620-19-9 exo-1,2,3,4-Tetrahydro-9-isopropyl-N-(4-methoxyphenyl)-1,4-iminonaphthalin-2,3-dicarboximid 
• 1265964-66-6 2-isopropyl-1-phenyisoindole 
• 1265964-63-3 2-isopropyl-1,3-diphenyisoindole 
• 123542-20-1 endo-1,2,3,4-Tetrahydro-9-isopropyl-N-(4-methylphenyl)-1,4-iminonaphthalin-2,3-dicarboximid 

Relevant academic research and scientific papers

Reduction of Benzolactams to Isoindoles via an Alkoxide-Catalyzed Hydrosilylation

An alkoxide-catalyzed reduction of benzolactams to isoindoles with silanes was realized. With t-BuOK as the catalyst and Ph2SiH2 as the reductant, a series of benzolactams containing different functional groups were reduced to the co

Cycloaddition-based formal C-H alkynylation of isoindoles leading to the synthesis of air-stable fluorescent 1,3-dialkynylisoindoles

Reaction of N-alkylisoindoles with (bromoethynyl)triisopropylsilane afforded 1,3-bis(triisopropylsilylethynyl) isoindoles in high yields. The formal C-H alkynylation proceeds under transition-metal-free conditions through [4 + 2] cycloaddition of the pyrrole ring of isoindole with bromoalkyne followed by ring-opening of the product.

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)

Studies on the Chemistry of Isoindoles and Isoindolenines, XXXVI. - Reactions of 2-Alkyl-2H-isoindoles with Maleic Imides

2-Alkyl-2H-isoindoles 2 react with maleic imides 4 exclusively in position 1 and 3 by cycloaddition to form Diels-Alder adducts.The transformation of the endo isomers 6 into the thermodynamically more stable exo isomers 7 depends on the dienophile.The cyc