The DOI matches its Crossref record; 9 of the 9 references it cites were found in a registry or an index.
A review of new developments in the Friedel–Crafts alkylation – From green chemistry to asymmetric catalysis
Open accessAbstract
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 processes. Additionally, the first diastereoselective and enantioselective Friedel–Crafts-type alkylations will be highlighted.
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Cites
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New Catalytic Approaches in the Stereoselective Friedel–Crafts Alkylation Reaction
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Abiotic synthesis of amino acids in the recesses of the oceanic lithosphere
Ménez, B., Pisapia, C., Andreani, M., Jamme, F., Vanbellingen, Q. P., Brunelle, A., Richard, L., Dumas, P., & Réfrégiers, M. (2018) · Nature · doi:10.1038/s41586-018-0684-z · Cited by 249
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Metadata
- Authors
- Rueping, M., & Nachtsheim, B. J.
- Venue
- Beilstein Journal of Organic Chemistry
- Publisher
- Beilstein Institut
- Published
- 2010-01-20
- Volume
- 6
- Pages
- 6-6
- ISSN
- 1860-5397 (ISSN-L)
- OpenAlex
- W2009170287
- Cited by
- 667
- References
- 9
- FWCI
- 12.30
- Type
- journal article
- Language
- en
- Open access
- diamond
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- Rueping, M., & Nachtsheim, B. J. (2010). A review of new developments in the Friedel–Crafts alkylation – From green chemistry to asymmetric catalysis. Beilstein Journal of Organic Chemistry. https://doi.org/10.3762/bjoc.6.6
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