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The synthesis of all-carbon-substituted, quaternary stereocenters through Lewis acid-catalyzed Friedel–Crafts alkylation of cyclic and acyclic 2-hydroxy oxime ethers proceeds under mild reaction conditions and with high yields. Moreover, the oxime ether moiety can be easily manipulated into various functional groups through subsequent modifications.

Graphical abstract: Lewis acid-catalyzed Friedel–Crafts reactions toward highly versatile, α-quaternary oxime ethers

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