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Cite the Following Article
Development of a continuous process for α-thio-β-chloroacrylamide synthesis with enhanced control of a cascade transformation
Olga C. Dennehy, Valérie M. Y. Cacheux, Benjamin J. Deadman, Denis Lynch, Stuart G. Collins, Humphrey A. Moynihan and Anita R. Maguire
Beilstein J. Org. Chem. 2016, 12, 2511–2522.
https://doi.org/10.3762/bjoc.12.246
How to Cite
Dennehy, O. C.; Cacheux, V. M. Y.; Deadman, B. J.; Lynch, D.; Collins, S. G.; Moynihan, H. A.; Maguire, A. R. Beilstein J. Org. Chem. 2016, 12, 2511–2522. doi:10.3762/bjoc.12.246
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- Kearney, A. M.; Murphy, L.; Murphy, C. C.; Eccles, K. S.; Lawrence, S. E.; Collins, S. G.; Maguire, A. R. Synthesis and reactivity of α-sulfenyl-β-chloroenones, including oxidation and Stille cross-coupling to form chalcone derivatives. Tetrahedron 2021, 88, 132091. doi:10.1016/j.tet.2021.132091
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- Dennehy, O. C.; Lynch, D.; Collins, S. G.; Maguire, A. R.; Moynihan, H. A. Scale-up and Optimization of a Continuous Flow Synthesis of an α-Thio-β-chloroacrylamide. Organic Process Research & Development 2020, 24, 1978–1987. doi:10.1021/acs.oprd.0c00079
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- Flynn, A. J.; Ford, A.; Khandavilli, U. B. R.; Lawrence, S. E.; Maguire, A. R. Regioselective Thermal [3+2]‐Dipolar Cycloadditions of α‐Diazoacetates with α‐Sulfenyl/Sulfinyl/Sulfonyl‐β‐Chloroacrylamide Derivatives to Form Densely Functionalised Pyrazoles. European Journal of Organic Chemistry 2019, 2019, 5368–5384. doi:10.1002/ejoc.201900494
- Huy, P.; Czekelius, C. 32.4.4 Chloro-, Bromo-, and Iodoalkenes (Update 2019). Knowledge Updates 2019/2; Georg Thieme Verlag KG, 2019. doi:10.1055/sos-sd-132-00171
- de Souza, B.; Keshavarz, L.; Steendam, R. R. E.; Dennehy, O. C.; Lynch, D.; Collins, S. G.; Moynihan, H. A.; Maguire, A. R.; Frawley, P. J. Solubility Measurement and Thermodynamic Modeling of N-(4-Methylphenyl-Z-3-chloro-2-(phenylthio)propenamide in 12 Pure Solvents at Temperatures Ranging from 278.15 to 318.15 K. Journal of Chemical & Engineering Data 2018, 63, 1419–1428. doi:10.1021/acs.jced.7b01011
- Kulkarni, A. A. Highlights from the Flow Chemistry Literature 2016 (Part 4). Journal of Flow Chemistry 2017, 7, 23–27. doi:10.1556/1846.2017.11111
