Efficient synthesis of 5'-O-laurate of 1-beta-D-arabinofuranosylcytosine via highly regioselective enzymatic acylation in binary solvent mixtures.

MLA

Li, Xiao-feng, et al. “Efficient Synthesis of 5’-O-Laurate of 1-Beta-D-Arabinofuranosylcytosine via Highly Regioselective Enzymatic Acylation in Binary Solvent Mixtures.” Bioorganic & Medicinal Chemistry Letters, vol. 20, no. 14, July 2010, pp. 4125–27. EBSCOhost, https://doi.org/10.1016/j.bmcl.2010.05.077.

APA

Li, X., Zong, M., & Zhao, G. (2010). Efficient synthesis of 5’-O-laurate of 1-beta-D-arabinofuranosylcytosine via highly regioselective enzymatic acylation in binary solvent mixtures. Bioorganic & Medicinal Chemistry Letters, 20(14), 4125–4127. https://doi.org/10.1016/j.bmcl.2010.05.077

Chicago

Li, Xiao-feng, Min-hua Zong, and Guang-lei Zhao. 2010. “Efficient Synthesis of 5’-O-Laurate of 1-Beta-D-Arabinofuranosylcytosine via Highly Regioselective Enzymatic Acylation in Binary Solvent Mixtures.” Bioorganic & Medicinal Chemistry Letters 20 (14): 4125–27. doi:10.1016/j.bmcl.2010.05.077.