862907-25-3

Basic information

• Product Name: 1-(tert-butoxycarbonyl)-2-oxo-3-phenylindolin-3-yl tert-butyl carbonate
• Synonyms: 1-(tert-butoxycarbonyl)-2-oxo-3-phenylindolin-3-yl tert-butyl carbonate
• CAS NO: 862907-25-3
• Molecular Weight: 425.481
• Mol File: 862907-25-3.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: 1-(tert-butoxycarbonyl)-2-oxo-3-phenylindolin-3-yl tert-butyl carbonate(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(tert-butoxycarbonyl)-2-oxo-3-phenylindolin-3-yl tert-butyl carbonate(862907-25-3)
• EPA Substance Registry System: 1-(tert-butoxycarbonyl)-2-oxo-3-phenylindolin-3-yl tert-butyl carbonate(862907-25-3)

Safety Data

• Hazardous Substances Data: 862907-25-3(Hazardous Substances Data)

Upstream product

• 108-86-1 bromobenzene 
• 139018-14-7 3-hydroxy-3-phenyl-1,3-dihydro-indol-2-one 
• 34619-03-9 tert-butyldicarbonate 
• 100-59-4 phenylmagnesium chloride 
• 24424-99-5 di-tert-butyl dicarbonate 
• 1402800-34-3 tert-butyl 3-hydroxy-2-oxo-3-phenylindoline-1-carboxylate 
• 160858-75-3 1-tert-butoxycarbonylisatin 
• 100-58-3 phenylmagnesium bromide 
• 91-56-5 indole-2,3-dione 

Downstream Products

• 862907-00-4 (R)-tert-butyl 3-fluoro-2-oxo-3-phenylindoline-1-carboxylate 
• 1040749-29-8 (S)-tert-butyl 3-fluoro-2-oxo-3-phenylindoline-1-carboxylate 
• 1351708-13-8 (S)-3-amino-3-phenylindolin-2-one 
• 1453221-33-4 (R)-tert-butyl 3-(2-formylethyl)-2-oxo-3-phenylindoline-1-carboxylate 
• 1567850-19-4 (S)-tert-butyl 3-phenyl-3-(trifluoromethanesulfenyl)-2-oxoindoline-1-carboxylate 
• 1567850-21-8 (R)-tert-butyl 3-phenyl-3-(trifluoromethanesulfenyl)-2-oxoindoline-1-carboxylate 
• 1289108-68-4 tert-butyl 3-(2-(1,3-dioxoisoindolin-2-yl)-3-ethoxy-3-oxopropyl)-2-oxo-3-phenylindoline-1-carboxylate 
• 1289108-15-1 tert-butyl 3-(2-(1,3-dioxoisoindolin-2-yl)-3-ethoxy-3-oxopropyl)-2-oxo-3-phenylindoline-1-carboxylate 
• 1289108-24-2 (R)-ethyl 2-acetamido-3-((S)-2-oxo-3-phenylindolin-3-yl)propanoate 
• 1289108-23-1 (R)-2-acetamido-3-((S)-2-oxo-3-phenylindolin-3-yl)propanoic acid 
• 1289108-21-9 C₂₃H₂₄N₂O₅ 

Relevant articles and documents

Electrochemical Umpolung C-H Functionalization of Oxindoles

Herein, we present a general electrochemical method to access unsymmetrical 3,3-disubstituted oxindoles by direct C-H functionalization where the oxindole fragment behaves as an electrophile. This Umpolung approach does not rely on stoichiometric oxidants and proceeds under mild, environmentally benign conditions. Importantly, it enables the functionalization of these scaffolds through C-O, and by extension to C-C or even C-N bond formation.

Asymmetric organocatalytic α-amination of 2-oxindoles with bis(2,2,2-trichloroethyl)azo-dicarboxylate

An enantioselective electrophilic amination of 3-substituted-2-oxindoles is reported, using bis(2,2,2-trichloroethyl)azo-dicarboxylate and commercially available Cinchona alkaloid organocatalysts. The best results were obtained in the reaction of 3-aryl s

Chincona alkaloid-catalyzed enantioselective trifluoromethylthiolation of oxindoles

An organocatalytic asymmetric trifluoromethylthiolation of 3-aryl or 3-alkyloxindoles employing a trifluoromethyl-substituted thioperoxide as the electrophilic trifluoromethylthiolating reagent was described. Reactions occurred in good to excellent enanti