Issue 15, 1972

New rearrangement in the quinoline series

Abstract

N-Lithio-1,2-dihydroquinolines (I) react with acid chlorides or esters to give the corresponding N-acylated derivatives (II), certain of which undergo rearrangement to the tertiary carbinols (III), in the presence of organolithium compounds.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1972, 865-866

New rearrangement in the quinoline series

C. E. Crawforth and O. Meth-Cohn, J. Chem. Soc., Chem. Commun., 1972, 865 DOI: 10.1039/C39720000865

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