17494-19-8

Upstream product

• 574-98-1 2-(2-bromoethyl)isoindoline-1,3-dione 
• 591-51-5 phenyllithium 
• 85-52-9 2-Benzoylbenzoic acid 
• 141-43-5 ethanolamine 

Downstream Products

• 97694-86-5 2-Furoylbenzophenone 
• 1159-86-0 o-dibenzoylbenzene 
• 85-52-9 2-Benzoylbenzoic acid 
• 5004-45-5 4-phenyl-2H-phthalazin-1-one 
• 18409-76-2 2-(1-phenyl-2,3-dihydro-1H-isoindol-2-yl)ethanol 
• 18409-77-3 2-(2-hydroxyethyl)-2,3-dihydro-3-phenylisoindol-1-one 
• 13669-70-0 nefopam 
• 84940-28-3 1-phenyl-3,4,5,6-tetrahydro-1H-2,5-benzoxazocine-5-carbonitrile 
• 10132-05-5 1,4-diphenyl-2,3-diazanaphthalene 
• 876065-68-8 2,3-dihydro-2-(2-phenylsulfanylethyl)-3-phenylisoindol-1-one 
• 876065-69-9 5,12b-dihydro-5-phenylthioisoindolo[1,2-a]isoquinolin-8(6H)-one 
• 876065-66-6 2,3-dihydro-3-phenyl-2-(2-phenylthioethyl)-isoindol-1-one 
• 876065-67-7 2-(2-chloroethyl)-2,3-dihydro-3-phenylisoindol-1-one 
• 876065-70-2 (1,3-dihydro-1-oxo-3-phenylisoindol-2-yl)acetaldehyde 

Relevant academic research and scientific papers

Oxidized isoquinolinoisoindolinone and benzazepinoisoindolinone alkaloids cores by convergent cyclisation processes: π-aromatic attack of thionium and oxonium species

An efficient methodology for synthesis of isoindoloisoquinoline 5a and isoindolobenzazepine 5b in oxidized forms as tetracyclic alkaloids cores are reported from N-bromoethylphthalimide (6) or phthalic anhydride and 2-phenylthioethylamine (8) in a five- o

Selective Non-Nucleoside HIV-1 Reverse Transcriptase Inhibitors. New 2,3-Dihydrothiazoloisoindol-5(9bH)-ones and Related Compounds with Anti-HIV-1 Activity

A series of substituted 2,3-dihydrothiazoloisoindol-5(9bH)-ones and related compounds 1-73 were synthesized and evaluated for their ability to inhibit reverse transcriptase (RT) of the human immune deficiency virus 1 (HIV-1) and replication of HIV-

The Reaction of Arylmagnesium Bromides with N-(ω-Bromoalkyl)phthalimides

The reaction of the N-(ω-bromoalkyl)phthalimides, 1 and 2, with a series of arylmagnesium bromides in tetrahydrofuran yielded the corresponding oxazoloisoindoles 4a-4h and oxazinoisoindoles 5a-5f.At low temperatures, phenylmagnesium bromide, on treatment

Synthesis and Reactions of 2,3-Dihydro-oxazoloisoindol-5(9bH)-ones

The synthesis and reactions with nucleophiles of 2,3-dihydro-oxazoloisoindol-5(9bH)-ones are described.

The Reaction of Lithium Phenylacetylide and Phenyllithium with N-(ω-Bromoalkyl)phthalimides

Lithium phenylacetylide reacted with short-chain N-(ω-bromoalkyl)phathalimides 1b and 1c to give tricyclic products 2b and 2c in moderate yields.Likewise, tricyclic products 3a-c were obtained when short-chain imides 1a-c were treated with phenyllithium.W