Synthesis and evaluation of 3'-azido-2',3'-dideoxypurine nucleosides as inhibitors of human immunodeficiency virus.

MLA

Zhang, Hong-Wang, et al. “Synthesis and Evaluation of 3’-Azido-2’,3’-Dideoxypurine Nucleosides as Inhibitors of Human Immunodeficiency Virus.” Bioorganic & Medicinal Chemistry Letters, vol. 20, no. 1, Jan. 2010, pp. 60–64. EBSCOhost, https://doi.org/10.1016/j.bmcl.2009.11.031.

APA

Zhang, H.-W., Coats, S. J., Bondada, L., Amblard, F., Detorio, M., Asif, G., Fromentin, E., Solomon, S., Obikhod, A., Whitaker, T., Sluis-Cremer, N., Mellors, J. W., & Schinazi, R. F. (2010). Synthesis and evaluation of 3’-azido-2’,3’-dideoxypurine nucleosides as inhibitors of human immunodeficiency virus. Bioorganic & Medicinal Chemistry Letters, 20(1), 60–64. https://doi.org/10.1016/j.bmcl.2009.11.031

Chicago

Zhang, Hong-Wang, Steven J Coats, Lavanya Bondada, Franck Amblard, Mervi Detorio, Ghazia Asif, Emilie Fromentin, et al. 2010. “Synthesis and Evaluation of 3’-Azido-2’,3’-Dideoxypurine Nucleosides as Inhibitors of Human Immunodeficiency Virus.” Bioorganic & Medicinal Chemistry Letters 20 (1): 60–64. doi:10.1016/j.bmcl.2009.11.031.