Radical methylation and radical hydroxymethylation of N-substituted quinoline derivatives.

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N-substituted quinoline derivatives such as 〓N+-Me, 〓N+O-, 〓N+-NH- were derived to methyl substituted compound at C-2 and/or C-4 by radical methylation and by radical hydroxymethylation. In the case of radical methylation and radical hydroxymethylation of quinoline 1-oxides, carbon at C-2 was preferentially nucleophilic than at C-4. Useful way to synthesize the alkyl substituted derivatives at C-2 selectively was to proceed the alkylation after forming N-oxide.

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