?SYNTHESIS OF HETERO-BICYCLIC COMPOUNDS Part-IX. Formation of 2,2-disubstituted 4,5-dioxo-pyridino [4,3-d] [1,3]dioxins

Authors

  • M.A. Butt PCSIR Laboratories Complex, Off University Road, Karachi-75280, Pakistan
  • R. KEMAL PCSIR Laboratories Complex, Off University Road, Karachi-75280, Pakistan
  • A. SALAM PCSIR Laboratories Complex, Off University Road, Karachi-75280, Pakistan
  • A AKHTAR PCSIR Laboratories Complex, Off University Road, Karachi-75280, Pakistan

Keywords:

Chloropyranodioxin, Pyridinodioxin, Hetero-bicycIiccompounds.

Abstract

Chloropyranodioxins (I) prepared by the reaction of malonyl chloride with mixed ketone were converted into 7-
(phenylamino)-pyranodioxins (II) which underwent the phenoxide rearrangement to yield the corresponding
pyridinodioxins (III), whose structures were determined by chemical conversions and spectroscopic studies.

Published

1997-10-20

How to Cite

Butt, M., KEMAL, R., SALAM, A., & AKHTAR, A. (1997). ?SYNTHESIS OF HETERO-BICYCLIC COMPOUNDS Part-IX. Formation of 2,2-disubstituted 4,5-dioxo-pyridino [4,3-d] [1,3]dioxins. Biological Sciences - PJSIR, 40(5-12), 1–4. Retrieved from https://v2.pjsir.org/index.php/biological-sciences/article/view/2339