A review of new developments in the Friedel–Crafts alkylation – From green chemistry to asymmetric catalysis
RWTH Aachen University · Harvard University Press
Abstract
The development of efficient Friedel-Crafts alkylations of arenes and heteroarenes using only catalytic amounts of a Lewis acid has gained much attention over the last decade. The new catalytic approaches described in this review are favoured over classical Friedel-Crafts conditions as benzyl-, propargyl- and allyl alcohols, or styrenes, can be used instead of toxic benzyl halides. Additionally, only low catalyst loadings are needed to provide a wide range of products. Following a short introduction about the origin and classical definition of the Friedel-Crafts reaction, the review will describe the different environmentally benign substrates which can be applied today as an approach towards greener…
Citation impact
- FWCI
- 15.04
- Percentile
- 100%
- References
- 131
Authors
2Topics & keywords
- Friedel–Crafts reaction
- Chemistry
- Alkylation
- Catalysis
- Organic chemistry
- Propargyl
- Enantioselective synthesis
- Halide
- Life in Land