PHOSPHORYLATION OF SOME NEW ACENAPHTHENEQUINONE DERIVATIVES

Authors

  • E. A. El-Sawi Chemistry Department, Faculty of Girls for Arts, Science and Education, Ain Shams University, Heliopolis, Cairo
  • T. B. Mostafa Chemistry Department, Faculty of Girls for Arts, Science and Education, Ain Shams University, Heliopolis, Cairo
  • H. A. Radwan Chemistry Department, Faculty of Girls for Arts, Science and Education, Ain Shams University, Heliopolis, Cairo

DOI:

https://doi.org/10.1007/6620

Keywords:

acenaphthenequinone, dioxadiazepine, epoxides, oxadiazole, phosphorane, phosphorylation

Abstract

Acenaphthenequinone reacted with diazofluorene, diphenyldiazomethane, phenylbenzoyldiazomethane, phenacyl chloride,  o-nitrobenzyl chloride, and diazohydroindenedione to give new oxadiazole,  ketoepoxide and dioxadiazepine derivatives. They  reacted with triphenylphosphine and triethylphosphite to give new organophosphorus compounds containing  a six-membered or four-membered phosphorane ring.  The structures were elucidated using IR, UV, NMR, and mass spectra, and elemental analyses.

How to Cite
El-Sawi, E. A.; Mostafa, T. B.; Radwan, H. A. Chem. Heterocycl. Compd. 2009, 45, 981. [Khim. Geterotsikl. Soedin. 2009, 1233.]

For this article in the English edition see DOI 10.1007/s10593-009-0363-y

 

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Published

2022-02-21

Issue

No. 8 (2009)

Section

Original Papers