Towers Tompkins, F. K., Parker, L. G., Fogarty, R. M., Seymour, J. M., Gousseva, E., Grinter, D. C., Palgrave, R. G., Smith, C. D. ORCID: https://orcid.org/0000-0002-5911-5836, Bennett, R. A. ORCID: https://orcid.org/0000-0001-6266-3510, Matthews, R. P. and Lovelock, K. R. J. ORCID: https://orcid.org/0000-0003-1431-269X (2024) Controlling and predicting alkyl-onium electronic structure. Chemical Communications, 60 (77). pp. 10756-10759. ISSN 1364-548X doi: https://doi.org/10.1039/D4CC03388D

Alshammari, A. A. A., Boyd, J. W., Greaves, N., Kettle, J. G., McKendrick, J. E. ORCID: https://orcid.org/0000-0003-2275-0569, Parker, L. G., Russell, A. T., Sani, A. and Smith, C. D. ORCID: https://orcid.org/0000-0002-5911-5836 (2024) Effect of tether length on endo/exo stereoselectivity in alkene–arene meta‐photocycloaddition reactions towards the Aphidocolin/Stemodin scaffolds. European Journal of Organic Chemistry. ISSN 1099-0690 doi: https://doi.org/10.1002/ejoc.202400463

Trunks, T. M., Babra, J. S., Westwood, J. and Smith, C. D. ORCID: https://orcid.org/0000-0002-5911-5836 (2022) A homocoupling approach to the key dione of CyMe4-BTPhen – vital ligands for nuclear clean-up by the SANEX process. SynOpen, 6 (1). pp. 16-18. ISSN 2509-9396 doi: https://doi.org/10.1055/a-1737-8610

Babra, J. S., Russell, A. T., Smith, C. D. ORCID: https://orcid.org/0000-0002-5911-5836 and Zhang, Y. (2018) Combining C-H functionalisation and flow photochemical heterocyclic metamorphosis (FP-HM) for the synthesis of benzo[1,3]oxazepines. Tetrahedron, 74 (38). pp. 5351-5357. ISSN 0040-4020 doi: https://doi.org/10.1016/j.tet.2018.05.066

Moore, J. S., Smith, C. D. ORCID: https://orcid.org/0000-0002-5911-5836 and Jensen, K. F. (2016) Kinetics analysis and automated online screening of aminocarbonylation of aryl halides in flow. Reaction Chemistry & Engineering, 1 (3). pp. 272-279. ISSN 2058-9883 doi: https://doi.org/10.1039/C6RE00007J

Sebastian, V., Smith, C. D. ORCID: https://orcid.org/0000-0002-5911-5836 and Jensen, K. F. (2016) Shape-controlled continuous synthesis of metal nanostructures. Nanoscale, 8 (14). pp. 7534-7543. ISSN 2040-3364 doi: https://doi.org/10.1039/c5nr08531d

Cranwell, P. B. ORCID: https://orcid.org/0000-0001-7156-5576, Russell, A. T. and Smith, C. D. ORCID: https://orcid.org/0000-0002-5911-5836 (2016) Methyl hydrazinocarboxylate as a practical alternative to hydrazine in the Wolff–Kishner reaction. Synlett, 27 (1). pp. 131-135. ISSN 0936-5214 doi: https://doi.org/10.1055/s-0035-1560805

Heublein, N., Moore, J. S., Smith, C. D. ORCID: https://orcid.org/0000-0002-5911-5836 and Jensen, K. F. (2014) Investigation of Petasis and Ugi reactions in series in an automated microreactor system. RSC Advances, 4. pp. 363627-63631. ISSN 2046-2069 doi: https://doi.org/10.1039/c4ra13626h

Smith, C. D. ORCID: https://orcid.org/0000-0002-5911-5836 and Greaney, M. F. (2013) Zinc mediated azide-alkyne ligation to 1,5- and 1,4,5-substituted 1,2,3-triazoles. Organic Letters, 15 (18). pp. 4826-4829. ISSN 1523-7060 doi: https://doi.org/10.1021/ol402225d

Smith, C. J., Smith, C. D. ORCID: https://orcid.org/0000-0002-5911-5836, Nikbin, N., Ley, S. V. and Baxendale, I. R. (2011) Flow synthesis of organic azides and the multistep synthesis of imines and amines using a new monolithic triphenylphosphine reagent. Organic and Biomolecular Chemistry, 2011 (9). pp. 1927-1937. ISSN 1477-0520 doi: https://doi.org/10.1039/c0ob00813c

Baxendale, I.R., Ley, S.V., Smith, C. ORCID: https://orcid.org/0000-0002-5911-5836, Tamborini, L. and Voica, A.F. (2008) A bifurcated pathway to thiazoles and imidazoles using a modular flow microreactor. Journal of Combinatorial Chemistry, 10 (6). pp. 851-857. ISSN 1520-4774 doi: https://doi.org/10.1021/cc800070a

Baumann, M., Baxendale, I.R., Ley, S.V., Nikbin, N. and Smith, C. ORCID: https://orcid.org/0000-0002-5911-5836 (2008) Azide monoliths as convenient flow reactors for efficient Curtius rearrangement reactions. Organic and Biomolecular Chemistry, 6. pp. 1587-1593. ISSN 1477-0520 doi: https://doi.org/10.1039/b801634h

Baumann, M., Baxendale, I.R., Ley, S.V., Nikbin, N., Smith, C. ORCID: https://orcid.org/0000-0002-5911-5836 and Tierney, J.P. (2008) A modular flow reactor for performing Curtius rearrangements as a continuous flow process. Organic and Biomolecular Chemistry, 6. pp. 1577-1586. ISSN 1477-0520 doi: https://doi.org/10.1039/b801631n

Smith, C. ORCID: https://orcid.org/0000-0002-5911-5836, Baxendale, I.R., Lanners, S., Hayward, J.J., Smith, S.C. and Ley, S.V. (2007) [3 + 2] Cycloaddition of acetylenes with azides to give 1,4-disubstituted 1,2,3-triazoles in a modular flow reactor. Organic and Biomolecular Chemistry, 5. pp. 1559-1561. ISSN 1477-0520 doi: https://doi.org/10.1039/b702995k

Smith, C. ORCID: https://orcid.org/0000-0002-5911-5836, Baxendale, I.R., Tranmer, G.K., Baumann, M., Smith, S.C., Lewthwaite, R.A. and Ley, S.V. (2007) Tagged phosphine reagents to assist reaction work-up by phase-switched scavenging using a modular flow reactor. Organic and Biomolecular Chemistry, 5. pp. 1562-1568. ISSN 1477-0520 doi: https://doi.org/10.1039/b703033a

Baxendale, I.R., Ley, S.V., Smith, C. ORCID: https://orcid.org/0000-0002-5911-5836 and Tranmer, G.K. (2006) A flow reactor process for the synthesis of peptides utilizing immobilized reagents, scavengers and catch and release protocols. Chemical Communications. pp. 4835-4837. ISSN 1359-7345 doi: https://doi.org/10.1039/b612197g

Smith, C. ORCID: https://orcid.org/0000-0002-5911-5836, Tchabanenko, K., Adlington, R.M. and Baldwin, J.E. (2006) Synthesis of linked heterocycles via use of bis-acetylenic compounds. Tetrahedron Letters, 47 (19). pp. 3209-3212. ISSN 0040-4039 doi: https://doi.org/10.1016/j.tetlet.2006.03.052