Regioselectivity of Friedel-Crafts acylation of aromatic compounds with several cyclic anhydrides
✍ Scribed by Iwao Hashimoto; Takatoshi Kawaji; Florin D. Badea; Tsuyoshi Sawada; Shuntaro Mataka; Masashi Tashiro; Gouki Fukata
- Book ID
- 114996547
- Publisher
- Springer Netherlands
- Year
- 1996
- Tongue
- English
- Weight
- 622 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0922-6168
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📜 SIMILAR VOLUMES
Friedel-Crafts acylation is carried out with several aromatic substrates in the presence of an electrochemically active aluminium anode to minimize the inorganic reagents. Only a catalytic amount of AlCl 3 (5 mol %) is required to enable the anodic polarization of the aluminium electrode to promote
The stable and non-hygroscopic aluminum dodecatungstophosphate (AlPW 12 O 40 ), was found to be an effective catalyst (3 mol%) for the solvent-free Friedel-Crafts acylation of aromatic compounds with carboxylic acids in the presence of trifluoroacetic anhydride under mild reaction conditions.