Issue 8, 1975

Addition reactions of heterocyclic compounds. Part LX. Reactions of 2-substituted pyridines with acetylenic esters leading to quinolizines and pyrrolo[2,1,5-cd]indolizines

Abstract

The reaction of methyl (2-pyridyl)acetate with methyl propiolate gave quinolizine derivatives; (2-pyridyl)acetone and 1-(2-pyridyl)butan-2-one reacted similarly. 2-Acetylpyridine and ethyl pyridine-2-carboxylate reacted with methyl propiolate to yield pyrrolo[2,1,5-cd]indolizines. The structures of the products were deduced mainly from their u.v. and n.m.r. spectra.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1975, 740-743

Addition reactions of heterocyclic compounds. Part LX. Reactions of 2-substituted pyridines with acetylenic esters leading to quinolizines and pyrrolo[2,1,5-cd]indolizines

R. M. Acheson and J. Woollard, J. Chem. Soc., Perkin Trans. 1, 1975, 740 DOI: 10.1039/P19750000740

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