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Scandium and Copper Triflate-Catalysed Acylaminoalkylation and Friedel-Crafts Alkylation Reactions

Moharem T. El Gihani, Harry Heaney, Khamis F. Shuhaibar

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Abstract

(opens in new window) Buy Article (opens in new window) Permissions and Reprints (opens in new window) All articles of this category (opens in new window) Acylaminoalkylation cyclisation reactions and some Friedel-Crafts alkylation reactions can be carried out using scandium or copper triflate as the Lewis acid catalyst: scandium triflate can be recycled with no loss of catalytic activity. re-usable catalyst - α-methoxyamide - acyliminium ion

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(opens in new window) Buy Article (opens in new window) Permissions and Reprints (opens in new window) All articles of this category (opens in new window) Acylaminoalkylation cyclisation reactions and some Friedel-Crafts alkylation reactions can be carried out using scandium or copper triflate as the Lewis acid catalyst: scandium triflate can be recycled with no loss of catalytic activity. re-usable catalyst - α-methoxyamide - acyliminium ion

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Available abstract

(opens in new window) Buy Article (opens in new window) Permissions and Reprints (opens in new window) All articles of this category (opens in new window) Acylaminoalkylation cyclisation reactions and some Friedel-Crafts alkylation reactions can be carried out using scandium or copper triflate as the Lewis acid catalyst: scandium triflate can be recycled with no loss of catalytic activity. re-usable catalyst - α-methoxyamide - acyliminium ion

Key concepts: Trifluoromethanesulfonate, Scandium, Friedel–Crafts reaction, Chemistry, Alkylation, Catalysis, Copper, Lewis acids and bases

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