Abstract
An efficient entry into densely substituted fluorinated and perfluoroalkylated benzene derivatives via chemo- and regioselective Pd-catalyzed [4 + 2] cross-benzannulation is presented. The synthetic utility of these products for the synthesis of various aromatic and heteroaromatic compounds is also demonstrated. This strategy offers a viable and quite general alternative to existing fluorination and perfluoroalkylation methods for securing these valuable molecules.
Original language | English (US) |
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Pages (from-to) | 2562-2565 |
Number of pages | 4 |
Journal | Organic Letters |
Volume | 15 |
Issue number | 10 |
DOIs | |
State | Published - May 17 2013 |
Externally published | Yes |
ASJC Scopus subject areas
- Biochemistry
- Physical and Theoretical Chemistry
- Organic Chemistry