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• 7α-Methoxy-carbonyl-6,7,8,14-tetra-hydro-6,14-endo-ethenothebaine.

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• Treatment of Acute Pain in Patients on Naltrexone: A Narrative Review.

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• Opioid receptor selectivity profile change via isosterism for 14-O-substituted naltrexone derivatives.

  Zhang Y, Elbegdorj O, Yuan Y, Beletskaya IO, Selley DE. Zhang Y, et al. Bioorg Med Chem Lett. 2013 Jul 1;23(13):3719-22. doi: 10.1016/j.bmcl.2013.05.027. Epub 2013 May 16. Bioorg Med Chem Lett. 2013. PMID: 23721804 Free PMC article.
• Characterization of 6α- and 6β-N-heterocyclic substituted naltrexamine derivatives as novel leads to development of mu opioid receptor selective antagonists.

  Yuan Y, Li G, He H, Stevens DL, Kozak P, Scoggins KL, Mitra P, Gerk PM, Selley DE, Dewey WL, Zhang Y. Yuan Y, et al. ACS Chem Neurosci. 2011 Jul 20;2(7):346-51. doi: 10.1021/cn2000348. Epub 2011 May 6. ACS Chem Neurosci. 2011. PMID: 22816021 Free PMC article.