Publications

20. O. Yahiaoui, H. D. Patel, K. S. Chinner, L. F. Pašteka, T. Fallon, Stereomutation of Substituted Bullvalenes, Organic Letters, 2020, ASAP, doi:10.1021/acs.orglett.0c03470.

19. T. V. de Castro, O. Yahiaoui, R. A. Peralta, T. Fallon, V. Lee, J. H. George, Biomimetic Synthesis Enables the Structure Revision of Littordials E and F and Drychampone B, Organic Letters, 2020, doi/10.1021/acs.orglett.0c03156

18. W. Lording, T. Fallon, M. S. Sherburn, M. N. Paddon-Row, The Simplest Diels-Alder Reactions Are Not Endo-Selective, Chemical Science, 2020, https://doi.org/10.1039/D0SC04553E

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17. O. Yahiaoui, A. Almass, T. Fallon, Total Synthesis of Endiandric Acid J and Beilcyclone A from Cyclooctatetraene, Chemical Science, 2020, DOI: 10.1039/d0sc03073b

16. R. A. Peralta, M. T. Huxley, J. D. Evans, T. Fallon, H. Cao, M. He, X. S. Zhao, S. Agnoli, C. J. Sumby, C. J. Doonan, Highly Active Gas Phase Organometallic Catalysis Supported Within Metal-organic Framework Pores. J. Am. Chem. Soc. 2020, DOI 10.1021/jacs.0c05286.

15. Y. Guo, C. Empel, C. Pei, I. Atodiresei, T. Fallon, R. M. Koenigs, Photochemical Cyclopropanation of Cyclooctatetraene and (Poly-)unsaturated Carbocycles, Org. Lett. 2020, 22, 5126–5130. 10.1021/acs.orglett.0c01734

14. H. D. Patel, T.-H. Tran, C. J. Sumby, L. F. Pašteka, T. Fallon, Boronate Ester Bullvalenes, J. Am. Chem. Soc. 2020, 142, 3680–3685. https://doi.org/10.1021/jacs.9b12930  

Highlighted in C&EN News

13. L. A. M. Murray, T. Fallon, C. J. Sumby, J. H. George, Total Synthesis of Naphterpin and Marinone Natural Products, Org. Lett. 2019, 21, 8312–8315. https://doi.org/10.1021/acs.orglett.9b03095  

12. O. Yahiaoui, L. F. Pašteka, C. J. Blake, C. G. Newton, T. Fallon, Network Analysis of Substituted Bullvalenes, Org. Lett. 2019, 21, 9574–9578. https://doi.org/10.1021/acs.orglett.9b03737

11. O. Yahiaoui, L. F. Pašteka, B. Judeel, T. Fallon, Synthesis and Analysis of Substituted Bullvalenes, Angew. Chem. Int. Ed. 2018, 57, 2570–2574.  https://doi.org/10.1002/anie.201712157

​10. T. Fallon, T. Meek, Simplified “no-D” NMR Methods for Routine Analysis and Organometallic Reagent Concentration Determination. Org. Lett. 2018, 19, 5752-5755. https://doi.org/10.1021/acs.orglett.7b02665

Supervised Research

9. M. F. Saglam, T. Fallon, M. N. Paddon-Row, M. S. Sherburn, Discovery and Computational Rationalization of Diminishing Alternation in [n]Dendralenes. J. Am. Chem. Soc. 2016, 138, 1022–1032. https://doi.org/10.1021/jacs.5b11889

8. E. G. Mackay, C. G. Newton, H. Toombs-Ruane, E. J. Lindeboom, T. Fallon, A. C. Willis, M. N. Paddon-Row, M. S. Sherburn, [5]Radialene, J. Am. Chem. Soc. 2015, 137, 14653–14659. https://doi.org/10.1021/jacs.5b07445

7. M. Pareek, T. Fallon, M. Oestreich, Platinum(0)-Catalyzed Indolyne Insertion into Bis(pinacolato)diboron Followed by Site-Selective Suzuki-Miyaura Cross-Coupling, Org. Lett. 2015, 17, 2082–2085.  https://doi.org/10.1021/acs.orglett.5b00604

6. T. Fallon, M. Oestreich, A Constellation of Deuterium-Labeled Silanes as a Simple Mechanistic Probe not Requiring Absolute Configuration Determination, Angew. Chem. Int. Ed. 2015, 54, 12488-12491. https://doi.org/10.1002/anie.201500750

5. K. M. Redies, T. Fallon, M. Oestreich, En route to stable all-carbon-substituted silylenes: Synthesis and reactivity of a bis(α-spirocyclopropyl)silylene, Organometallics 2014, 33, 3235-3238. https://doi.org/10.1021/om500485m

4. T. Fallon, A. C. Willis, M. N. Paddon-Row, M. S. Sherburn, Furanodendralenes, J. Org. Chem. 2014, 79, 3185–3193. https://doi.org/10.1021/jo500458y

3. T. Fallon, A. C. Willis, A. D. Rae, M. N. Paddon-Row, M. S. Sherburn, β-Oligofurans, Chem. Sci. 2012, 3, 2133–2137. https://doi.org/10.1039/C2SC20130

2. H. Toombs-Ruane, N. Osinski, T. Fallon, C. Wills, A.C. Willis, M.N. Paddon-Row, M.S. Sherburn, Synthesis and applications of tricarbonyliron complexes of dendralenes. Chem. – Asian J. 2011, 6, 3243-3250. https://doi.org/10.1002/asia.201100455

1. T. Fallon, D. E. J. E. Robinson, A. C. Willis, M. N. Paddon-Row, M. S. Sherburn, Double dehydro-diels-alder reactions of 1,5-dien-3-ynes, Chem. Eur. J. 2010, 16, 760–765. https://doi.org/10.1002/chem.200902190