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Galmarini, C.M., Popowycz, F. and Joseph, B. (2008) Cytotoxic Nucleoside Analogues: Different Strategies to Improve Their Clinical Efficacy. Current Medicinal Chemistry, 15, 1072-1082.
.http://dx.doi.org/10.2174/092986708784221449

has been cited by the following article:

• TITLE: Synthesis and X-Ray Structure of Important Anticancer Nucleosides Intermediate (2R,3S,4S,5R)-2-(acetoxymethyl)-5- (3-bromo-5-(methoxycarbonyl)- 1H-1,2,4-triazol-1-yl)tetrahydrofuran- 3,4-diyl Diacetate

  AUTHORS: Yang Liu, Guanghui Tian, Hongguang Ge, Xiaoyan Cao, Daihua Hu, Dehua Zhang

  KEYWORDS: Anticancer Nucleosides, Intermediate, Triazole Nucleosides

  JOURNAL NAME: Journal of Crystallization Process and Technology, Vol.4 No.3, June 30, 2014

  ABSTRACT: An important anticancer nucleosides intermediate (2R,3S,4S,5R)-2-(acetoxymethyl)-5-(3-bromo-5-(methoxycar-bonyl)-1H-1,2,4-triazol-1-yl)tetrahydrofuran-3,4-diyl diacetate was synthesized by directly coupling the bromotriazole with the protected ribose sugar, and have given the corresponding product in moderate yield. Its structure and conformation were confirmed by single crystal X-ray diffraction.