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- Title
Frontispiece: Redox‐Neutral Tetrafluoroethylation of Aryl Alkynes with 1,1,2,2‐Tetrafluoroethane Sulfonic Acid Leading to α‐Tetrafluoroethylated Acetophenones.
- Authors
Kawamoto, Takuji; Noguchi, Kohki; Takata, Ryotaro; Sasaki, Rio; Matsubara, Hiroshi; Kamimura, Akio
- Abstract
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.
- Subjects
ACETOPHENONE; ALKYNES; SULFONIC acids
- Publication
Chemistry - A European Journal, 2021, Vol 27, Issue 37, p1
- ISSN
0947-6539
- Publication type
Academic Journal
- DOI
10.1002/chem.202183763