Synthesis of New Nucleoside Analogues from Theobromine

Authors

  • Thanaa M Al-Mouamin
  • Sumaya J Abid

Keywords:

Nucleoside Analogues, theobromine, mercury salt

Abstract

Nucleoside Analogues play important role in different medical drugs,therefor we synthesized new nucleoside analogues using theobromine as a nucleobase, for the first time, by convertion to it's mercury salt, [1]. Then coupled with three kinds of sugar, including (glucose, galactose and mannose), after protection [2-4] and activation as bromo sugar [5-7] afforded blocked nucleoside analogues [8-10] which subsequently hydrolyzed to give our synthetic goal the free nucleoside analogues [11-13]. All prepared compounds were identify by FT-IR and some of them with 1H-NMR spectroscopy. The synthesized compounds (11-13) were screened for their in-vitro antibacterial and antifungal activity.

Published

2019-01-10

Issue

Section

Articles

How to Cite

[1]
“Synthesis of New Nucleoside Analogues from Theobromine”, ANJS, no. 2, pp. 17–29, Jan. 2019, Accessed: Mar. 28, 2024. [Online]. Available: https://anjs.edu.iq/index.php/anjs/article/view/2045