1. Micellar Catalysis of the Suzuki Miyaura Reaction using Biogenic Pd Nanoparticles from Desulfovibrio alaskensis. Y. Era, J. A. Dennis, S. Wallace*, L. E. Horsfall*, Green Chem. 2021, Advance Article - link

  2. Microbial Synthesis of Vanillin from Waste poly(ethylene terephthalate). J. C. Sadler, S. Wallace*, Green Chem. 2021, 23, 4665–4672 - link - press release

  3. Interfacing Non-Enzymatic Catalysis with Living Microorganisms. J. C. Sadler, J. A. Dennis, N. W. Johnson, S. Wallace*, RSC Chem. Biol. 2021, 2, 1073–1083 - link 

  4. Optimizing the Biosynthesis of Oxygenated and Acylated Taxol Precursors in Saccharomyces cerevisiae using Advanced Bioprocessing Strategies. L. E. Walls, K. Malci, B. Nowrouzi, R. A. Li, L. d'Espaux, J. Wong, J. A. Dennis, A. J. C. Semiao, S. Wallace, J. L. Martinez, J. D. Keasling, L. Rios-Solis, Biotechnol. Bioeng. 2020, 118, 279–293 - link

  5. One-Pot Synthesis of Adipic Acid from Guaiacol in Escherichia coli. J. T. Suitor, S. Varzandeh, S. Wallace*, ACS Synth. Biol. 2020, 9, 2472–2476 - link - press release 

  6. Transition Metal-Free Reduction of Activated Alkenes Using a Living Microorganism. R. C. Brewster, J. T. Suitor, A. W. Bennett, S. Wallace*, Angew. Chem. Int. Ed. 2019, 58, 12409–12414 - link

  7. Synthetic Methodologies in Chemical Biology. In book: Biomolecular and Bioanalytical Techniques: Theory, Methodology and Applications. R. C. Brewster, S. Wallace*. John Wiley & Sons, Inc. Editor: V. Ramesh, 2019, ISBN: 9781119483977

  8. Computationally Guided Discovery of a Reactive, Hydrophilic trans-5-Oxocene Dienophile for Bioorthogonal Labeling. W. D Lambert, S. L. Scinto, O. Dmittrenko, S. J. Boyd, R. A. Mehl, J. W. Chin*, J. M. Fox*, S. Wallace*, Org. Biomol. Chem. 2017, 15, 6640–6644 - link

  9. Protein Modification via Alkyne Hydrosilylation Using a Substoichiometric Amount of Ruthenium(II) Catalyst. T. T. L. Kwan, O. Boutureira, E. C. Frye, S. J. Walsh, M. K. Gupta, S. Wallace, Y. Wu, F. Zhang, H. F. Sore, W. R. J. D. Galloway, J. W. Chin, M. Welch, G. J. L. Bernardes, D. R. Spring, Chem. Sci. 2017, 8, 3871–3878 - link

  10. Interfacing Biocompatible Reactions with Engineered Escherichia coli. S. Wallace, E. P. Balskus, Methods Mol. Biol. 2017, 1586, 409–421 - link

  11. Designer Micelles Accelerate Flux Through Engineered Metabolism and Support Biocompatible Chemistry. S. Wallace, E. P. Balskus, Angew. Chem. Int. Ed. 2016, 55, 6023–6027 - link

  12. Interfacing Microbial Styrene Production with a Biocompatible Cyclopropanation Reaction. S. Wallace, E. P. Balskus, Angew. Chem. Int. Ed. 2015, 54, 7106–7109 - link

  13. Using Non-Enzymatic Chemistry to Influence Microbial Metabolism. S. Wallace, E. E. Shultz, E. P. Balskus, Curr. Opin. Chem. Biol. 2015, 25, 71–79 - link

  14. Opportunities for Merging Chemical and Biological Synthesis. S. Wallace, E. P. Balskus, Curr. Opin. Biotechnol. 2014, 30, 1–8 - link

  15. Strain-Promoted Sydnone Bicyclo-[6.1.0]-nonyne Cycloaddition. S. Wallace, J.  W. Chin, Chem. Sci. 2014, 5, 1742–1744 - link

  16. Conformationally Strained trans-Cyclooctene with Improved Stability and Excellent Reactivity in Tetrazine Ligation. A. Darko, S. Wallace, O. Dmitrenko, M. M. Machovina, R. A. Mehl, J. W. Chin, J. M. Fox, Chem. Sci. 2014, 5, 3770–3776 - link

  17. Optimized Orthogonal Translation of Unnatural Amino Acids Enables Spontaneous Protein Double-Labeling and FRET. K. Wang, A. Sachdeva, D. J. Cox, N. W. Wilf, S. Wallace, R. A. Mehl, J. W. Chin, Nat. Chem. 2014, 6, 393–403 - link

  18. A Cascade Strategy Enables a Total Synthesis of (–)-Gephyrotoxin. S. Chu, S. Wallace, M. D. Smith, Angew. Chem. Int. Ed. 2014, 53, 13826–13829 - link

  19. Genetic Encoding of Bicyclononynes and trans-Cyclooctenes for Site-Specific Protein Labeling in vitro and in Live Mammalian Cells. K. Lang, L. Davis, S. Wallace, M. Mahesh, D. J. Cox, M. L. Blackman, J. M. Fox, J. W. Chin, J. Am. Chem. Soc. 2012, 134, 10317–10320 - link

  20. Rapid Synthesis and Zebrafish Evaluation of a Phenanthridine-Based Small Molecule Library. L. R. Donaldson, S. Wallace, D. Haigh, E. E. Paton, A. N. Hulme, Org. Biomol. Chem. 2011, 9, 2233–2239 - link