Synthesis of essramycin and comparison of its antibacterial activity
Ernest H L Tee1, Tomislav Karoli, Soumya Ramu
1Institute for Molecular Bioscience, University of Queensland, St Lucia, Queensland 4072, Australia.
Journal of Natural Products
|November 6, 2010
Abstract:
The triazolopyrimidine natural product essramycin (1) was synthesized without the use of protecting groups via a two-step reaction scheme involving a 3-amino-1,2,4-triazole intermediate, and its structure was unequivocally determined. However, in contrast to the natural product, the synthetic essramycin (1) did not display any antibacterial activity.
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