42899-83-2

Upstream product

• 117-21-5 3-chlorophthalic anhydride 
• 62-53-3 aniline 
• 4727-29-1 phthalanilic acid 
• 51108-30-6 4-chloro-1H-isoindole-1,3(2H)-dione 
• 591-50-4 iodobenzene 

Downstream Products

• 80564-18-7 2-phenyl-4-chloro-1,3-dithiophthalimide 
• 66294-34-6 2-phenyl-4-chloro-1-thiophthalimide 
• 80564-23-4 2-phenyl-1-benzylimino-4-chloro-3-oxoisoindoline 
• 66294-33-5 4,4'-dichloro-2,2'-diphenyl-[1,1']biisoindolylidene-3,3'-dione 
• 80564-36-9 (Z)-4,4'-Dichloro-2,2'-diphenyl-[1,1']biisoindolylidene-3,3'-dithione 
• 1207091-08-4 3-ethylthio-N-phenylphthalimide 
• 1207091-09-5 3-ethylsulfonyl-N-phenylphthalimide 
• 18241-62-8 3-ethylsulfonylphthalic acid 
• 6832-92-4 3-chloro-N-phenylbenzamide 
• 36978-37-7 3,3',4,4'-biphenyltetracarboxylic acid tetramethyl ester 
• 18245-63-1 3-ethylthiophthalic acid 
• 890411-32-2 3-mercapto-N-phenylphthalimide 
• 58974-88-2 3,3'-bis(n-phenylphthalimide) sulfide 

Relevant academic research and scientific papers

Ru-Catalyzed Selective C-H Bond Hydroxylation of Cyclic Imides

We report on cyclic imides as weak directing groups for selective monohydroxylation reactions using ruthenium catalysis. Whereas acyclic amides are known to promote the hydroxylation of the C(sp2)-H bond enabling five-membered ring ruthenacycle intermediates, the cyclic imides studied herein enabled the hydroxylation of the C(sp2)-H bond via larger six-membered ruthenacycle intermediates. Furthermore, monohydroxylated products were exclusively obtained (even in the presence of overstoichiometric amounts of reagents), which was rationalized by the difficulty to accommodate coplanar intermediates once the first hydroxyl group was introduced into the substrate. The same reactivity was observed in the presence of palladium catalysts.

NOVEL COMPOUND AND ORGANIC LIGHT EMITTING DEVICE COMPRISING THE SAME

The present invention relates to a novel compound capable of improving efficiency and low driving voltage and/or lifespan characteristics in an organic light emitting device; and an organic light emitting device including the same. The compound is represe

Unmasking Amides: Ruthenium-Catalyzed Protodecarbonylation of N-Substituted Phthalimide Derivatives

The unprecedented transformation of a wide range of synthetically appealing phthalimides into amides in a single-step operation has been achieved in high yields and short reaction times using a ruthenium catalyst. Mechanistic studies revealed a unique, homogeneous pathway involving five-membered ring opening and CO2 release with water being the source of protons.

Visible-light induced isoindoles formation to trigger intermolecular diels-alder reactions in the presence of air

Visible-light induced isoindole formation triggered an intermolecular Diels-Alder reaction with dienophiles such as acetylenedicarboxylate and maleimides in the presence of air. The reaction resulted in excellent diastereoselctivity and high yields under

Insecticidal Benzenedicarboxamide Derivative

The present invention relates to a novel benzenedicarboxamide derivative and the use thereof as an insecticide having the formula (I) wherein the chemical groups W1 to W9, and R1 to R3 are as defined here-in.

Monothio- and Dithio-phthalimides: Part V - Synthesis of Chlorinated β-Isoindigo and Dithio-β-isoindigo Derivatives

The reaction of chlorinated monothio- and dithio-phthalimides (II and III) with amines in equimolar amounts in acetic acid gives 2-aryl-1-arylimino-4-chloro-3-oxoisoindolines (IV) and 2-aryl-1-arylimino-4-chloro-3-thioisoindolines (V), respectively.Compou