CONVENIENT APPROACH TO SYNTHESIS OF ALKALOID CERPEGIN DERIVATIVESv

Authors

  • A.A. Hovhannisyan Chair of Organic Chemistry, YSU, Armenia

DOI:

https://doi.org/10.46991/PYSU:B/2014.48.1.003

Keywords:

cerpegin, pyridinealkaloid, 2-oxo-2,5-dihydrofuran, furo[3,4-c]- pyridine-3,4-dione

Abstract

A convenient method for obtaining pyridine alkaloid cerpegin and its various new C-1 and N-5 derivatives in high yields has been developed. Starting enaminolactones, synthesized by means of various tertiary keto-alcohols, have been condensed with primary aliphatic, aromatic or heterocyclic amines for a pyridine cycle formation. Bromine derivatives of furo[3,4-c]pyridinenones are obtained as well.

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Published

2014-03-17

How to Cite

Hovhannisyan, A.A. 2014. “CONVENIENT APPROACH TO SYNTHESIS OF ALKALOID CERPEGIN DERIVATIVESv”. Proceedings of the YSU B: Chemical and Biological Sciences 48 (1 (233):3-9. https://doi.org/10.46991/PYSU:B/2014.48.1.003.

Issue

Vol. 48 No. 1 (233) (2014)

Section

Chemistry

License

Copyright (c) 2014 Proceedings of the YSU

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This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.