Publications

Journal Articles

  1. A. M. ElSohly, J. I. MacDonald, N. B. Hentzen, I. L. Aanei, K. M. El Muslemany, and M. B. Francis. ortho-Methoxyphenols as Convenient Oxidative Coupling Reagents with Application to Site-Selective Heterobifunctional Crosslinkers. J. Am. Chem. Soc. 2017, 139, 3767-3773.
  2. I. L. Aanei, A. M. ElSohly, C. Netirojjanakul, M. Regan, S. Taylor-Murphy, M. E. Farkas, J. P. O’Neil, Y. Seo, and M. B. Francis. Biodistribution of Antibody-MS2 Viral Capsid Conjugates in Breast Cancer Models. Mol. Pharm. 2016, 13, 3764-3772.
  3. A. M. ElSohly, C. Netirojjanakul, I. L. Aanei, A. Jager, S. C. Bendall, M. E. Farkas, G. P. Nolan, and M. B. Francis. Synthetically Modified Viral Capsids as Versatile Carriers for Use in Antibody-based Cell Targeting. Bioconjugate Chem. 2015, 26, 1590–1596.
  4. A. M. ElSohly and M. B. Francis. Development of Oxidative Coupling Strategies for Site-Selective Protein Modification. Acc. Chem. Res. 2015, 48, 1971–1978.
  5. S. L. Capehart, A. M. ElSohly, A. C. Obermeyer, and M. B. Francis. Bioconjugation of Gold Nanoparticles through the Oxidative Coupling of ortho-Aminophenols and Anilines. Bioconjugate Chem. 2014, 25, 1888–1892.
  6. K. M. El Muslemany, A. A. Twite, A. M. ElSohly, A. C. Obermeyer, R. Mathies, and M. B. Francis. Photoactivated Bioconjugation between ortho-Azidophenols and Anilines: A Facile Approach to Biomolecular Photopatterning. J. Am. Chem. Soc. 2014, 136, 12600–12606.
  7. N. E. Wright, A. M. ElSohly, and S. A. Snyder. Syntheses of Cyclotriveratrylene Analogs and Their Long Elusive Triketone Congeners. Org. Lett. 2014, 16, 3644–3647.
  8. A. M. ElSohly, D. A. Wespe, T. J. Poore, and S. A. Snyder. An Efficient Approach to the Securinega Alkaloids Empowered by Cooperative N-Heterocyclic Carbene/Lewis Acid Catalysis. Angew. Chem. Int. Ed. 2013, 52, 5789–5794.
  9. S. A. Snyder, A. M. ElSohly, and F. Kontes. Synthetic Approaches to Oligomeric Natural Products. Nat. Prod. Rep. 2011, 28, 897–924.
  10. S. A. Snyder, F. Kontes, and A. M. ElSohly. Mechanistic Investigations of the Cyclocondensation Step of the Knorr Pyrrole Synthesis. Heterocycles 2011, 84, 265–274.
  11. S. A. Snyder, A. M. ElSohly, and F. Kontes. Synthetic and Theoretical Investigations of Myrmicarin Biosynthesis. Angew. Chem. Int. Ed. 2010, 49, 9693–9698.
  12. A. M. ElSohly, B. W. Hopkins, K. L. Copeland, and G. S. Tschumper. Anchoring the potential energy surface of the diacetylene dimer. Mol. Phys. 2009, 107, 923–928.
  13. A. M. ElSohly and G. S. Tschumper. Comparison of Polarization Consistent and Correlation Consistent Basis Sets for Noncovalent Interactions. Int. J. Quantum Chem. 2009, 109, 91–96.
  14. A. M. ElSohly, C. L. Shaw, M. E. Guice, B. D. Smith, and G. S. Tschumper. Analytic Gradients for the Multicentered Integrated QM:QM Method for Weakly Bound Clusters: Efficient and Accurate 2-Body:Many-Body Geometry Optimizations. Mol. Phys. 2007, 105, 2777–2782.
  15. B. W. Hopkins, A. M. ElSohly, and G. S. Tschumper. Reliable Structures and Energetics for Two New Delocalized π···π Prototypes: Cyanogen Dimer and Diacetylene Dimer. Phys. Chem. Chem. Phys. 2007, 9, 1550–1558.
  16. A. M. ElSohly, M. L. Renault, and G. S. Tschumper. Reliable Electron Affinities of Perfluorocyclopropane and Perfluorocyclobutane from Convergent ab Initio Computations. J. Phys. Chem. A 2006, 110, 1975–1977.
  17. A. M. ElSohly, G. S. Tschumper, R. A. Crocombe, J. T. Wang, and T. F. Williams. Computational and ESR Studies of Electron Attachment to Decafluorocyclopentane, Octafluorocyclobutane, and Hexafluorocyclopropane: Electron Affinities of the Molecules and the Structures of their Stable Negative Ions as Determined from the 13C and 19F Hyperfine Coupling Constants. J. Am. Chem. Soc. 2005, 127, 10573–10583.

 

Book Chapters

  1. A. M. ElSohly and M. B. Francis “Antibody Modification of p-Aminophenylalanine-Containing Proteins.” Chapter 15 in Methods in Molecular Biology (Ed. Andrew K. Udit) Springer, Los Angeles, 2018.

 

Patents

  1. M. B. Francis, A. M. ElSohly, and A. Ogunkoya. “Detection of Cannabinoids Using a Sensitive Fluorescence Assay.” Provisional Patent in preparation.

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