82875-60-3

Upstream product

• 75-24-1 trimethylaluminum 
• 121680-77-1 (R)-(+)-2,3,4,5,6-pentafluorostyrene oxide 
• 711-44-4 1-methyl-2',3',4',5',6'-pentafluorostyrene 
• 13561-85-8 1,2-Epoxy(pentafluorphenyl)ethan 

Downstream Products

• 719-30-2 2-(Pentafluorophenyl)propionic acid 
• 134225-26-6 C₁₀H₇F₅O 
• 134225-26-6 C₁₀H₇F₅O 
• 781-26-0 (-)-2-(pentafluorophenyl)propionyl chloride 

Relevant academic research and scientific papers

An exceptional hydroboration of substituted fluoroolefins providing tertiary alcohols

Figure presented A rare hydroboration-oxidation providing 3°-alcohols has been achieved in the case of 1,1,2-perfluoroalkyl(aryl)ethylenes. The hydroboration of substituted perfluoroalkyl(aryl)ethylenes with dichloroborane reveals that the regioselectivit

Pentafluorophenyl derivatives, methods of production thereof, and method of optical resolution of chiral carboxylic acids

Pentafluorophenyl derivatives are expressed by the formula (I): STR1 where X represents an alkyl group having from 1 to 4 carbon atoms or a halogen atom; Y represents any group of --CH2 OH, --COOH, --COCl, --CON1 R2, or --

Asymmetric synthesis of α-methyl carboxylic acid derivatives stereochemistry in acidic ring opening of epoxides

Optically active α-methyl carboxylic acid derivatives were prepared via reaction of microbially produced epoxides with trimethylaluminum. Stereochemistry of the ring opening reaction was discussed through an MO calculation.