Enzymatic synthesis and phosphorolysis of 4(2)-thioxo- and 6(5)-azapyrimidine nucleosides by E. coli nucleoside phosphorylases

Vladimir A. Stepchenko, Anatoly I. Miroshnikov, Frank Seela and Igor A. Mikhailopulo
Beilstein J. Org. Chem. 2016, 12, 2588–2601. https://doi.org/10.3762/bjoc.12.254

Supporting Information

Supporting Information File 1: Analytical and computational data.
Format: PDF Size: 872.8 KB Download

Cite the Following Article

Enzymatic synthesis and phosphorolysis of 4(2)-thioxo- and 6(5)-azapyrimidine nucleosides by E. coli nucleoside phosphorylases
Vladimir A. Stepchenko, Anatoly I. Miroshnikov, Frank Seela and Igor A. Mikhailopulo
Beilstein J. Org. Chem. 2016, 12, 2588–2601. https://doi.org/10.3762/bjoc.12.254

How to Cite

Stepchenko, V. A.; Miroshnikov, A. I.; Seela, F.; Mikhailopulo, I. A. Beilstein J. Org. Chem. 2016, 12, 2588–2601. doi:10.3762/bjoc.12.254

Download Citation

Citation data can be downloaded as file using the "Download" button or used for copy/paste from the text window below.
Citation data in RIS format can be imported by all major citation management software, including EndNote, ProCite, RefWorks, and Zotero.

Presentation Graphic

Picture with graphical abstract, title and authors for social media postings and presentations.
Format: PNG Size: 201.7 KB Download

Citations to This Article

Up to 20 of the most recent references are displayed here.

Scholarly Works

  • Zhou, X.; Yan, W.; Zhang, C.; Yang, Z.; Neubauer, P.; Mikhailopulo, I. A.; Huang, Z. Biocatalytic synthesis of seleno-, thio- and chloro-nucleobase modified nucleosides by thermostable nucleoside phosphorylases. Catalysis Communications 2019, 121, 32–37. doi:10.1016/j.catcom.2018.12.004
  • Ding, Q. Enzymatic and Chemical Synthesis of Nucleic Acid Derivatives; Wiley, 2018; pp 129–157. doi:10.1002/9783527812103.ch6
  • Downey, A. M.; Hocek, M. Strategies toward protecting group-free glycosylation through selective activation of the anomeric center. Beilstein journal of organic chemistry 2017, 13, 1239–1279. doi:10.3762/bjoc.13.123
Other Beilstein-Institut Open Science Activities