1596355-39-3

Basic information

• Product Name: ethyl (3S)-3-[(3S)-2,5-dioxo-1-phenylpyrrolidin-3-yl]-2-oxo-1-(prop-2-en-1-yl)-2,3-dihydro-1H-indole-3-carboxylate
• Synonyms: ethyl (3S)-3-[(3S)-2,5-dioxo-1-phenylpyrrolidin-3-yl]-2-oxo-1-(prop-2-en-1-yl)-2,3-dihydro-1H-indole-3-carboxylate
• CAS NO: 1596355-39-3
• Molecular Weight: 418.449
• Mol File: 1596355-39-3.mol

Chemical Properties

• CAS DataBase Reference: ethyl (3S)-3-[(3S)-2,5-dioxo-1-phenylpyrrolidin-3-yl]-2-oxo-1-(prop-2-en-1-yl)-2,3-dihydro-1H-indole-3-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl (3S)-3-[(3S)-2,5-dioxo-1-phenylpyrrolidin-3-yl]-2-oxo-1-(prop-2-en-1-yl)-2,3-dihydro-1H-indole-3-carboxylate(1596355-39-3)
• EPA Substance Registry System: ethyl (3S)-3-[(3S)-2,5-dioxo-1-phenylpyrrolidin-3-yl]-2-oxo-1-(prop-2-en-1-yl)-2,3-dihydro-1H-indole-3-carboxylate(1596355-39-3)

Safety Data

• Hazardous Substances Data: 1596355-39-3(Hazardous Substances Data)

Upstream product

• 146852-20-2 1-allyl-1,3-dihydro-2H-indol-2-one 
• 941-69-5 N-phenyl-maleimide 

Relevant articles and documents

Efficient asymmetric Michael reaction of 2-oxindole-3-carboxylate esters with maleimides catalyzed by cinchonidine

A highly efficient enantioselective Michael reaction of 2-oxindole-3-carboxylate esters with N-maleimides catalyzed by commercially available cinchonidine was described. The desired adducts, containing a quaternary center at the C3-position and a vicinal tertiary center, were obtained in excellent yields (up to 99%), good enantioselectivities (up to 85% ee), and diastereoselectivities (dr>90:10) in the presence of 0.05-5 mol % catalyst loading.