32566-02-2

Upstream product

• 1176667-12-1 C₁₆H₁₀ClF₃N₂O 
• 784183-51-3 N-(4-chloro-2-iodophenyl)-2,2,2-trifluoroacetamide 
• 41994-44-9 5-chloro-2-nitrobenzoyl chloride 
• 155249-86-8 2-(5-Chloro-2-nitro-phenyl)-1H-indole 

Downstream Products

• 238398-40-8 2-(2-acetylamino-5-chlorophenyl)indole 
• 1449134-95-5 1-((2'R,3'S)-3',6-dichloro-2-phenylspiro[benzo[d][1,3]oxazine-4,2'-indolin]-1'-yl)ethanone 
• 1449135-07-2 N-(2-(1-acetyl-1H-indol-2-yl)-4-chlorophenyl)benzamide 
• 238398-46-4 2-(2-acetylamino-5-chlorophenyl)-3-nitrosoindole 
• 238398-52-2 2-(2-amino-5-chlorophenyl)-3-nitrosoindole 

Relevant academic research and scientific papers

Palladium(II)-catalyzed cycloamidination via C(sp2)-H activation and isocyanide insertion

An efficient method for the synthesis of nitrogen heterocycles containing a cyclic amidine moiety has been developed. The process involves palladium-catalyzed C(sp2)-H activation and isocyanide insertion starting with readily accessible ortho-heteroarene-substituted aniline derivatives under mild conditions. Copyright

Platinum-catalyzed formal Markownikoff's hydroamination/hydroarylation cascade of terminal alkynes assisted by tethered hydroxyl groups

(Chemical Equation Presented) An efficient method for Markownikoff's hydroamination-hydroarylation of alkynols using PtBr2 as catalyst has been developed. The platinum-catalyzed reactions of alkynols with amino group containing aromatics were a

Polycondensed nitrogen heterocycles. Part 27. Indolo[3,2-c]cinnoline. Synthesis and antileukemic activity

Indolo[3,2-c]cinnolines of type 5, variously substituted either in the indole and in the cinnoline moieties, were prepared in good overall yields, by intramolecular cyclization of indolo derivatives 4. Compounds 5a-d showed a good cytotoxic activity again