Liang, Apeng’s team published research in Chemical Communications (Cambridge, United Kingdom) in 2012 | 832735-54-3

Chemical Communications (Cambridge, United Kingdom) published new progress about Boronic acids, esters Role: RCT (Reactant), RACT (Reactant or Reagent) (aryl/heteroaryl). 832735-54-3 belongs to class pyridine-derivatives, and the molecular formula is C18H22BNO3, Name: 2-(Benzyloxy)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine.

Liang, Apeng; Li, Xinjian; Liu, Dongfeng; Li, Jingya; Zou, Dapeng; Wu, Yangjie; Wu, Yusheng published the artcile< The palladium-catalyzed cross-coupling reactions of trifluoroethyl iodide with aryl and heteroaryl boronic acid esters>, Name: 2-(Benzyloxy)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine, the main research area is aryl boronic acid ester trifluoroethyl iodide cross coupling palladium; heteroaryl boronic acid ester trifluoroethyl iodide cross coupling palladium; trifluoroethyl arene preparation; palladium cross coupling catalyst.

The cross-coupling reactions of 1,1,1-trifluoro-2-iodoethane with aryl and heteroaryl boronic acid esters have been successfully achieved. The new protocol allows for a convenient introduction of trifluoroethyl groups into a variety of aryl and heteroaryl moieties under mild conditions.

Chemical Communications (Cambridge, United Kingdom) published new progress about Boronic acids, esters Role: RCT (Reactant), RACT (Reactant or Reagent) (aryl/heteroaryl). 832735-54-3 belongs to class pyridine-derivatives, and the molecular formula is C18H22BNO3, Name: 2-(Benzyloxy)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine.

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem