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Perfluoroalkylation of Unactivated Alkenes with Acid Anhydrides as the Perfluoroalkyl Source
- Source :
- Angewandte Chemie International Edition. 55:8740-8743
- Publication Year :
- 2016
- Publisher :
- Wiley, 2016.
-
Abstract
- An efficient perfluoroalkylation of unactivated alkenes with perfluoro acid anhydrides was developed. Copper salts play a crucial role as a catalyst to achieve allylic perfluoroalkylation with the in situ generated bis(perfluoroacyl) peroxides. Furthermore, carboperfluoroalkylation of alkene bearing an aromatic ring at an appropriate position on the carbon side chain was found to proceed under metal-free conditions to afford carbocycles or heterocycles bearing a perfluoroalkyl group. This method, which makes use of readily available perfluoroalkyl sources, offers a convenient and powerful tool for introducing a perfluoroalkyl group onto an sp(3) carbon to construct synthetically useful skeletons.
- Subjects :
- chemistry.chemical_classification
Allylic rearrangement
010405 organic chemistry
Chemistry
Alkene
chemistry.chemical_element
Homogeneous catalysis
General Medicine
General Chemistry
010402 general chemistry
Ring (chemistry)
01 natural sciences
Peroxide
Catalysis
0104 chemical sciences
chemistry.chemical_compound
Side chain
Organic chemistry
Carbon
Subjects
Details
- ISSN :
- 14337851
- Volume :
- 55
- Database :
- OpenAIRE
- Journal :
- Angewandte Chemie International Edition
- Accession number :
- edsair.doi.dedup.....8ce9d1085011d44a42c2b7bfc456c513
- Full Text :
- https://doi.org/10.1002/anie.201604127