1449291-35-3

Upstream product

• 31541-32-9 1-(4-methoxybenzyl)-1H-indole-2,3-dione 
• 1400636-03-4 3-allyl-3-hydroxy-1-(4-methoxybenzyl)indolin-2-one 
• 104-55-2 3-phenyl-propenal 

Relevant academic research and scientific papers

Kinetic resolution of tertiary alcohols: Highly enantioselective access to 3-hydroxy-3-substituted oxindoles

Enantioselective: The first highly enantioselective kinetic resolution of 3-hydroxy-3-substituted oxindoles has been developed through oxidative esterification catalyzed by a N-heterocyclic carbene (see picture). This method uses a simple procedure and provides 3-hydroxy-oxindoles with various substituents at the 3-position in excellent enantiopurity. S=selectivity. Copyright