112274-46-1

Upstream product

• 110330-40-0 benzoic acid-{2-[1-(methyl-phenyl-hydrazono)-ethyl]-anilide} 
• 32566-01-1 2-(2-aminophenyl)-1H-indole 
• 52670-38-9 2-ethynylaniline 
• 698-02-2 N,N-dimethyl-o-iodoaniline 
• 101350-36-1 N-(2-(1-methyl-1H-indol-2-yl)phenyl)carboxamide 
• 65610-86-8 2-(2-aminophenyl)-1-methyl-1H-indole 
• 882495-09-2 2-(2-isocyanophenyl)-1-methyl-1H-indole 
• 98-80-6 phenylboronic acid 
• 551-93-9 2-aminoacetophenone 
• 618-40-6 1-Methyl-1-phenylhydrazine 
• 40754-13-0 2-(1-(2-phenylhydrazineylidene)ethyl)aniline 

Relevant academic research and scientific papers

Selective CH or NH Imidoylative Annulation of 2-(2-Isocyanophenyl)-1H-indoles Leading to Diverse Indole-fused Scaffolds

2-(2-Isocyanophenyl)-1H-indoles, a class of functionalized isocyanides containing both aromatic CH and indolo NH functionalities, are first applied in selective imidoylative annulation reactions. Scaffolds of 6-aryl 11H-indolo[3,2-c]quinoline and 6-aryl i

Cu(OTf)2-Catalyzed Intramolecular Radical Cascade Reactions for the Diversity-Oriented Synthesis of Quinoline-Annulated Polyheterocyclic Frameworks

Compound libraries with high levels of structural diversity and novelty could cover underexploited chemical space and thus have been highly pursued in drug discovery. Herein, we report the first Cu(OTf)2-catalyzed intramolecular radical cascade reactions

Selective C?H or N?H Imidoylative Annulation of 2-(2-Isocyanophenyl)-1H-indoles Leading to Diverse Indole-fused Scaffolds

2-(2-Isocyanophenyl)-1H-indoles, a class of functionalized isocyanides containing both aromatic C?H and indolo N?H functionalities, are first applied in selective imidoylative annulation reactions. Scaffolds of 6-aryl 11H-indolo[3,2-c]quinoline and 6-aryl