79485-25-9Relevant articles and documents
Electrolytic partial fluorination of organic compounds. 20. Electrosynthesis of novel hypervalent iodobenzene chlorofluoride derivatives and its application to indirect anodic gem-difluorination
Fujita, Toshiyasu,Fuchigami, Toshio
, p. 4725 - 4728 (1996)
Electrosynthesis of novel hypervalent iodobenzene chlorofluorides was successfully performed for the first time and it was demonstrated that p-methoxyiodobenzene chlorofluoride could be used as a mediator for indirect anodic gem-difluorination of dithioacetals.
Electrolytic Partial Fluorination of Organic Compounds. 14. The First Electrosynthesis of Hypervalent Iodobenzene Difluoride Derivatives and Its Application to Indirect Anodic gem-Difluorination
Fuchigami, Toshio,Fujita, Toshiyasu
, p. 7190 - 7192 (2007/10/02)
The electrosynthesis of hypervalent iodobenzene difluorides was accomplished by anodic oxidation of p-nitro- and p-methoxyiodobenzenes with Et3N*3HF in anhydrous acetonitrile, and p-methoxyiodobenzene difluoride was used as a mediator for indirect anodic
Stable Carbenium Ions, 26. - Diarylfluorocarbenium Ions - 19F-NMR-spectroscopic Determination of Substituent Effects in p-substituted Diarylcarbenium Ions
Volz, Heinrich,Mayer, Wilhelm Dietrich
, p. 1407 - 1414 (2007/10/02)
Diarylfluorocarbenium hexafluoroantimonates have been prepared as crystalline salts and are characterised.The 19F-chemical shift of the methine fluoroatom is used as a measure of the relative stability of the studied carbenium ions.The relations of this m