Frontispiece: Redox‐Neutral Tetrafluoroethylation of Aryl Alkynes with 1,1,2,2‐Tetrafluoroethane Sulfonic Acid Leading to α‐Tetrafluoroethylated Acetophenones.

Kawamoto, Takuji; Noguchi, Kohki; Takata, Ryotaro; Sasaki, Rio; Matsubara, Hiroshi; Kamimura, Akio

DFT calculations, radicals, reaction mechanisms, synthetic methods, tetrafluoroethylation Keywords: DFT calculations; radicals; reaction mechanisms; synthetic methods; tetrafluoroethylation EN DFT calculations radicals reaction mechanisms synthetic methods tetrafluoroethylation 1 1 1 07/05/21 20210702 NES 210702 B Redox-neutral tetrafluoroethylation b of aryl alkynes with 1,1,2,2-tetrafluoroethane sulfonic acid leading to -tetrafluoroethylated acetophenones is described in the Full Paper by Takuji Kawamoto and co-workers on page 9529 ff. Frontispiece: Redox-Neutral Tetrafluoroethylation of Aryl Alkynes with 1,1,2,2-Tetrafluoroethane Sulfonic Acid Leading to -Tetrafluoroethylated Acetophenones.

ACETOPHENONE; ALKYNES; SULFONIC acids

Chemistry - A European Journal, 2021, Vol 27, Issue 37, p1

0947-6539

Academic Journal

10.1002/chem.202183763