1351708-13-8

Basic information

• Product Name: (S)-3-amino-3-phenylindolin-2-one
• Synonyms: (S)-3-amino-3-phenylindolin-2-one
• CAS NO: 1351708-13-8
• Molecular Weight: 224.262
• Mol File: 1351708-13-8.mol

Chemical Properties

• CAS DataBase Reference: (S)-3-amino-3-phenylindolin-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-3-amino-3-phenylindolin-2-one(1351708-13-8)
• EPA Substance Registry System: (S)-3-amino-3-phenylindolin-2-one(1351708-13-8)

Safety Data

• Hazardous Substances Data: 1351708-13-8(Hazardous Substances Data)

Upstream product

• 3456-79-9 3-phenyloxindole 
• 91-56-5 indole-2,3-dione 
• 862907-25-3 1-(tert-butoxycarbonyl)-2-oxo-3-phenylindolin-3-yl tert-butyl carbonate 
• 862906-97-6 tert-butyl 2-oxo-3-phenylindoline-1-carboxylate 
• 139018-14-7 3-hydroxy-3-phenyl-1,3-dihydro-indol-2-one 
• 100-59-4 phenylmagnesium chloride 

Relevant articles and documents

Rhodium-Catalyzed Enantioselective Addition of Arylboroxines to Isatin-Derived N-Boc Ketimines Using Chiral Phosphite-Olefin Ligands: Asymmetric Synthesis of 3-Aryl-3-amino-2-oxindoles

An efficient rhodium-catalyzed enantioselective arylation of isatin-derived N-Boc ketimines with arylboroxines has been developed using H8-BINOL-derived phosphite-olefin as a chiral ligand. This method allows access to a broad variety of valuab

Bifunctional thiourea-modified polymers of intrinsic microporosity for enantioselective α-amination of 3-aryl-2-oxindoles in batch and flow conditions

Two novel polymers of intrinsic microporosity decorated with chiral thioureas have been used as recoverable organocatalysts in enantioselective α-amination of 3-aryl-substituted oxindoles, creating a quaternary stereocenter. Both catalysts were able to pr

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

Organocatalytic asymmetric α-amination of unprotected 3-aryl and 3-aliphatic substituted oxindoles using di-tert-butyl azodicarboxylate

The bifunctional quinine-derived thiourea catalyst 14 was found to catalyze the direct amination of unprotected 3-aryl and aliphatic substituted oxindoles with di-tert-butyl azodicarboxylate (DBAD) to construct a tetrasubstituted stereogenic carbon center at the C-3 position of oxindoles in good to excellent yield and enantioselectivity. Copyright