Issue 0, 1971

Organolithium chemistry of N-heterocycles. Part III. Reduction of 2-methylquinoline by lithium in tetrahydrofuran

Abstract

Treatment of 2-methylquinoline with lithium in tetrahydrofuran at 0° gives a dimeric product (IV). From this several reduced dimers have been obtained [(II), (III) and (V)]. The reduction of 2,6-dimethylquinoline proceeds in a similar manner.

Article information

Article type
Paper

J. Chem. Soc. C, 1971, 2453-2457

Organolithium chemistry of N-heterocycles. Part III. Reduction of 2-methylquinoline by lithium in tetrahydrofuran

A. M. Jones, C. A. Russell and O. Meth-Cohn, J. Chem. Soc. C, 1971, 2453 DOI: 10.1039/J39710002453

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