58995-87-2

Upstream product

• 1301267-80-0 N-{2-[(2-aminophenyl)ethynyl]phenyl}benzamide 
• 220396-46-3 (1H-indol-2-yl)boronic acid 
• 615-36-1 2-bromoaniline 
• 40754-13-0 2-(1-(2-phenylhydrazineylidene)ethyl)aniline 
• 32566-01-1 2-(2-aminophenyl)-1H-indole 
• 98-88-4 benzoyl chloride 
• 613-90-1 benzoyl cyanide 
• 88207-42-5 2-(2-nitrophenyl)-1-phenylsulphonylindole 
• 88207-43-6 2-(2-aminophenyl)-1-phenylsulphonylindole 
• 59050-53-2 2-(2-nitrophenyl)-1H-indole 
• 88207-44-7 2-(2-benzamidophenyl)-1-phenylsulphonylindole 

Downstream Products

• 110423-27-3 6-phenyl-indolo[1,2-c]quinazoline 
• 1449135-20-9 1-((2'R)-3'-hydroxy-2-phenylspiro[benzo[d][1,3]oxazine-4,2'-indolin]-1'-yl)ethanone 
• 1449135-19-6 (2'R,3'R)-1'-acetyl-2-phenylspiro[benzo[d][1,3]oxazine-4,2'-indolin]-3'-yl nitrate 
• 1449134-96-6 (2'R,3'S)-tert-butyl 3'-chloro-2-phenylspiro[benzo[d][1,3]oxazine-4,2'-indoline]-1'-carboxylate 
• 1449134-85-3 1-((2'R,3'S)-3'-chloro-2-phenylspiro[benzo[d][1,3]oxazine-4,2'-indolin]-1'-yl)ethanone 
• 1449135-08-3 tert-butyl 2-(2-benzamidophenyl)-1H-indole-1-carboxylate 
• 1449134-97-7 N-(2-(1-acetyl-1H-indol-2-yl)phenyl)benzamide 

Relevant academic research and scientific papers

HETEROCYCLIC COMPOUND AND ORGANIC LIGHT EMITTING DEVICE COMPRISING THE SAME

The present invention relates to a heterocyclic compound represented by chemical formula 1 and an organic light emitting device comprising the same. According to the present invention, the heterocyclic compound represented by the chemical formula 1 may be

Enantioselective chlorocyclization of indole derived benzamides for the synthesis of spiro-indolines

(DHQD)2PHAL catalyzed enantioselective chlorocyclization of indole derived benzamides was realized. Spiro-indolines containing a continuous quaternary carbon center and tertiary carbon center were obtained in good yields with excellent enantioselectivity (up to 90% yield and 96% ee).

Facile assembly of 11 H -indolo[3,2-c]quinoline by a two-step protocol involving a regioselective 6- endo -cyclization promoted by the hendrickson reagent

An expedient approach was developed to construct the 11H-indolo[3,2-c] quinoline scaffold starting from acyclic alkyne substrates. The five- and six-membered nitrogen-containing rings in the tetracyclic skeleton were elaborated efficiently by gold(III)-ca

Indole β-Nucleophilic Substitution. Part 7. β-Halogenation of Indoles. Attempted Intramolecular β-Nucleophilic Substitution of α-Arylindoles

Intramolecular β-nucleophilic substitution of 2-aryl-1-phenylsulphonylindoles could not be achieved.N-Arylsulphonylation of 2-arylindoles with arylsulphonyl halides using phase-transfer conditions is accompanied by 3-halogenation in some cases; the propor

2-Phenyl-indole derivatives and process for preparing the same

New stabilizers of polymers and co-polymers of vinyl chloride, the said stabilizers being 2-phenyl-indole derivatives corresponding to the formula: STR1 wherein R represents a phenyl radical, an amino group, optionally substituted by an acetyl or benzoyl