KnowraFriedel–Crafts reactionLinked fromLinked fromThe 14 pages that link to Friedel–Crafts reaction, each with the reason it gives.All 14Broader topic 2Related 11Narrower topic 1Lewis acidRelated: Aluminum chloride commonly acts as a Lewis acid to generate the reactive electrophile.Iron(III) chlorideRelated: Iron(III) chloride can activate halides as a Lewis acid in some Friedel–Crafts reactions.Aluminium chlorideRelated: AlCl₃ commonly activates alkyl or acyl halides in these carbon–carbon bond-forming reactions.Phthalic anhydrideRelated: Early phthalic anhydride synthesis used Friedel–Crafts chemistry to build an aromatic precursor.Boron trifluorideRelated: BF₃ can activate reagents as a Lewis acid in Friedel–Crafts chemistry.Organosilicon chemistryRelated: Early organosilicon synthesis adapted classical electrophilic methods to make arylsilicon compounds.Titanium tetrachlorideRelated: TiCl₄ can act as a Lewis-acid promoter in selected Friedel–Crafts reactions.Triflic acidRelated: Triflic acid can promote these reactions by generating or activating electrophiles.Antimony trichlorideRelated: SbCl₃ can act as a Lewis acid in some Friedel–Crafts reactions.Tin(IV) chlorideRelated: Tin(IV) chloride can promote these reactions by activating electrophilic reagents.AzuleneRelated: Friedel–Crafts chemistry has been used in routes to substituted azulenes and azulene frameworks.