New cyclopenta[b]-pyrroles and -pyridines by reaction of 2-azido- and 2-phosphoranylideneaminocyclopent-1-ene-1-carbaldehydes with aliphatic esters
- 1 January 1989
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Perkin Transactions 1
- No. 8,p. 1369-1373
- https://doi.org/10.1039/p19890001369
Abstract
A new cyclopenta [b]pyrrole has been synthesized by reaction of 2-azidocyclopent-1-ene-1-carbaldehyde with ethyl acetate and subsequent thermal cyclisation. Dicyclopenta [b,e] pyrazines have been isolated from a similar reaction with ethyl propionate or t-butyl propionate. Condensation of the corresponding iminophosphorane from 2-azidocyclopent-1-ene-1-carbaldehyde with ethyl acetate and cyclisation of the dienic iminophosphorane so obtained gave a cyclopenta[b]pyridine. The products were characterized on the basis of 1H n.m.r., i.r., and mass spectrometric results.This publication has 2 references indexed in Scilit: