1233369-73-7

Basic information

• Product Name: (+)-tert-butyl 3-(1-(3-bromophenyl)-2,5-dioxopyrrolidin-3-yl)-2-oxo-3-phenylindoline-1-carboxylate
• CAS NO: 1233369-73-7
• Molecular Weight: 561.432
• Mol File: 1233369-73-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (+)-tert-butyl 3-(1-(3-bromophenyl)-2,5-dioxopyrrolidin-3-yl)-2-oxo-3-phenylindoline-1-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: (+)-tert-butyl 3-(1-(3-bromophenyl)-2,5-dioxopyrrolidin-3-yl)-2-oxo-3-phenylindoline-1-carboxylate(1233369-73-7)
• EPA Substance Registry System: (+)-tert-butyl 3-(1-(3-bromophenyl)-2,5-dioxopyrrolidin-3-yl)-2-oxo-3-phenylindoline-1-carboxylate(1233369-73-7)

Safety Data

• Hazardous Substances Data: 1233369-73-7(Hazardous Substances Data)

Upstream product

• 862906-97-6 tert-butyl 2-oxo-3-phenylindoline-1-carboxylate 
• 53534-14-8 N-(3-bromophenyl)maleimide 

Relevant articles and documents

Highly diastereo- and enantioselective michael additions of 3-substituted oxindoles to maleimides catalyzed by chiral bifunctional thiourea-tertiary amine

A highly diastereo- and enantioselective Michael addition reaction with respect to prochiral 3-substituted oxindoles and maleimides by a chiral bifunctional thiourea-tertiary amine catalyst was investigated for the first time. The corresponding adducts, containing a quaternary center at the C3-position of the oxindole as well as a vicinal tertiary center, were generally obtained in good to high yields (up to 92%) with high to excellent diastereo- (up to 99:1 dr) and enantioselectivities (up to 99% ee).