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N-Methylisoquinolinium iodide

Isoquinolones. When N-methylisoquinolinium iodide (1) in f-butyl alcohol is treated with solid KOH and then oxygenated, N-methylisoquinolone (2) is obtained in 827o yield. The oxidation is believed to involve the pseudo base a. The choice of solvent is important, but the substituent on nitrogen does not affect the yield. Also, the reaction appears to be general for heterocyclic iminium salts. ... [Pg.188]

N-Methylisoquinolinium iodide allowed to react with 2,6-dichlorobenzaldehyde and NaBH4 in dimethylformamide 4-(2,6-didilorobenzyl)-2-methyl-1,2-di-... [Pg.501]

See other pages where N-Methylisoquinolinium iodide is mentioned: [Pg.336]    [Pg.446]   
See also in sourсe #XX -- [ Pg.366 , Pg.367 ]



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2-Methylisoquinolinium iodide

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