Issue 0, 1980

Addition reactions of heterocyclic compounds. Part 70. Formation of quinolizines and indolizines from nicotine derivatives and acetylenic esters

Abstract

Cotinine and other nicotine derivatives have been converted to 9aH- and 4H-quinolizines by dimethyl acetylenedicarboxylate, while cotinine itself by a series of steps has yielded 6-(1-methyl-5-oxopyrrolidin-2-yl)indolizine.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1980, 78-80

Addition reactions of heterocyclic compounds. Part 70. Formation of quinolizines and indolizines from nicotine derivatives and acetylenic esters

R. M. Acheson, M. J. Ferris and N. M. Sinclair, J. Chem. Soc., Perkin Trans. 1, 1980, 78 DOI: 10.1039/P19800000078

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