A regio- and stereo-controlled approach to triazoloquinoxalinyl C-nucleosides

作者：Amer Adel^*; Ayoup Mohammed Salah; Khattab Sherine Nabil; Hassan Seham Yassen; Langer Vratislav; Senior Samir; El Massry Abdel Moneim

来源：Carbohydrate Research, 2010, 345(17): 2474-2484.

DOI：10.1016/j.carres.2010.08.010

• Acyclic triazoloquinoxalinyl C-nucleosides
• Cyclic triazoloquinoxalinyl C-nucleosides
• Antimicrobial activity
• Tautomerism

The synthesis of a new series of acyclic triazoloquinoxalinyl C-nucleosides and their transformation to their cyclic analogs are described following protection, activation, and deprotection with subsequent intramolecular nucleophilic substitution protocol. The antibacterial potency of the new compounds was determined using an inhibition zone diameter test. The results show that 3a and 2b exhibit good activity against Escherichia coli and Candida albicans. On the other hand, the cyclic mesylated C-nucleoside 13 showed activity against the Gram-positive bacteria (Staphylococcus aureus) and antifungal activity against C. albicans.

• 出版日期2010-11-22