Pleschke, A’s team published research in Journal of Fluorine Chemistry in 2004-06-30 | 1435-43-4

Journal of Fluorine Chemistry published new progress about Aryl chlorides Role: RCT (Reactant), RACT (Reactant or Reagent). 1435-43-4 belongs to class chlorides-buliding-blocks, and the molecular formula is C6H3ClF2, Computed Properties of 1435-43-4.

Pleschke, A.; Marhold, A.; Schneider, M.; Kolomeitsev, A.; Roschenthaler, G.-V. published the artcile< Halex reactions of aromatic compounds catalysed by 2-azaallenium, carbophosphazenium, aminophosphonium and diphosphazenium salts: a comparative study>, Computed Properties of 1435-43-4, the main research area is fluoride aryl preparation; chloride aryl halogen exchange azaallenium carbophosphazenium aminophosphonium diphosphazenium catalyst.

One of the most common methods to introduce fluorine into aromatic compounds is the well-investigated halogen-exchange (Halex) reaction, in which chloro- and bromoaroms. activated towards nucleophilic substitution, react with a fluoride source to yield the corresponding fluoroarenes. In general, the reaction is supported by phase-transfer catalysts. The new classes of compounds, I (X = C, R = Me; X = Et2NP, R = Et), were found to be active phase-transfer catalysts allowing for substitution of even weakly activated halogens.

Journal of Fluorine Chemistry published new progress about Aryl chlorides Role: RCT (Reactant), RACT (Reactant or Reagent). 1435-43-4 belongs to class chlorides-buliding-blocks, and the molecular formula is C6H3ClF2, Computed Properties of 1435-43-4.

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics