Correction to Reduction Sensitive Lipid Conjugates of Tenofovir

Apr 17, 2017 - missing an oxygen atom to the immediate left of the stereogenic center. The upper left structure should feature a. “propyl” ether, ...
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Addition/Correction pubs.acs.org/jmc

Correction to Reduction Sensitive Lipid Conjugates of Tenofovir: Synthesis, Stability, and Antiviral Activity Kyle E. Giesler,* Jose Marengo, and Dennis C. Liotta* Journal of Medicinal Chemistry 2016, 59, 7097−7110. DOI: 10.1021/acs.jmedchem.6b00428 Page 7097. In the abstract graphic, all of the structures are missing an oxygen atom to the immediate left of the stereogenic center. The upper left structure should feature a “propyl” ether, not an “ethyl”. The bottom structure should have an aliphatic chain length of 16 carbon atoms immediately left of the disulfide, not 13. The correct abstract graphic is shown below:

Page 7098. In Figure 1, the structure of compound 1 (CMX157) should feature a “propyl” ether, not an “ethyl” ether. The correct Figure 1 is shown below:

Page 7098: In Figure 2, the structure is missing an oxygen atom to the immediate left of the stereogenic center. The correct Figure 2 is shown below:

© XXXX American Chemical Society

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DOI: 10.1021/acs.jmedchem.7b00537 J. Med. Chem. XXXX, XXX, XXX−XXX