94027-63-1

Upstream product

• 107519-49-3 (3-chloro-2-oxo-indolin-3-yl)-phenyl-acetonitrile 
• 7677-24-9 trimethylsilyl cyanide 
• 23782-37-8 (3E)-3-benzylidene-1,3-dihydro-2H-indol-2-one 
• 613-90-1 benzoyl cyanide 
• 220466-11-5 1-isocyanato-2-(2-phenylethynyl)benzene 
• 140-29-4 phenylacetonitrile 
• 101291-04-7 2-(3-hydroxy-2-oxoindolin-3-yl)-2-phenylacetonitrile 

Downstream Products

• 101290-92-0 (R/S)-2-(2-oxoindolin-3-yl)-2-phenylacetonitrile 
• 5027-78-1 2-phenyl-2-(3-indolyl)-1-aminoethane 
• 3335-81-7 3-(2-amino-1-phenyl-ethyl)-1,3-dihydro-indol-2-one 
• 1262120-82-0 C₁₆H₁₂N₂O₂ 

Relevant academic research and scientific papers

CeCl3·7H2O catalyzed C(sp2)?CN bond construction on water: Synthesis of (Z)-2-(2-Oxoindolin-3-ylidene)-2-arylacetonitriles

An environmentally friendly method for the construction of C(sp2)–CN bond on water has been described, and (Z)-2-(2-oxoindolin-3-ylidene)-2-arylacetonitriles were synthesized by using CeCl3· 7H2O as a catalyst. The reactio

Stereoselective synthesis of 3-(1-Cyanoalkylidene)oxindoles by palladium-catalyzed cyclization reaction of 2-(Alkynyl)aryl isocyanates with copper(I) cyanide

A palladium-catalyzed cyclization reaction of 2-(alkynyl)-aryl isocyanates with copper(I) cyanide provides an efficient method for the stereoselective synthesis of (Z)-configured 3-(1-cyanoalkylidene)oxindoles.