Riley, William; Jones, Andrew C.; Singh, Kuldip; Browne, Duncan L.; Stuart, Alison M. published the artcile< Accessing novel fluorinated heterocycles with the hypervalent fluoroiodane reagent by solution and mechanochemical synthesis>, Application In Synthesis of 1391728-13-4, the main research area is flurotetrahydropyridazine preparation; unsaturated tosyl hydrazone fluoroiodane mediated regioselective intramol fluorocyclization; fluro dihydrooxazine preparation; unsaturatedketoxime fluoroiodane mediated regioselective intramol flurocyclization.
A new and efficient strategy for the rapid formation of novel fluorinated tetrahydropyridazines and dihydrooxazines were developed by fluorocyclisation of β,γ-unsaturated hydrazones and oximes with the fluoroiodane reagent. Mechanochem. synthesis delivered fluorinated tetrahydropyridazines in similar excellent yields to conventional solution synthesis, whereas fluorinated dihydrooxazines were prepared in much better yields by ball-milling.
Chemical Communications (Cambridge, United Kingdom) published new progress about Alcohols, unsaturated Role: RCT (Reactant), RACT (Reactant or Reagent). 1391728-13-4 belongs to class iodides-buliding-blocks, and the molecular formula is C9H10FIO, Application In Synthesis of 1391728-13-4.
Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com