Supporting Information
The experimental section describing the preparation of all new compounds, the copies of the NMR data (1H NMR, 13C NMR, 19F NMR), HOESY and NOESY experiments and crystallographic data for compounds 1d, 4d and 25. The CIF files of 1d, 4d and 25.
Supporting Information File 1: Experimental section and copies of spectra. | ||
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Supporting Information File 2: Crystallographic data (cif) for compounds E-1d, E-4d, and Z-25. | ||
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Cite the Following Article
Selective preparation of tetrasubstituted fluoroalkenes by fluorine-directed oxetane ring-opening reactions
Clément Q. Fontenelle, Thibault Thierry, Romain Laporte, Emmanuel Pfund and Thierry Lequeux
Beilstein J. Org. Chem. 2020, 16, 1936–1946.
https://doi.org/10.3762/bjoc.16.160
How to Cite
Fontenelle, C. Q.; Thierry, T.; Laporte, R.; Pfund, E.; Lequeux, T. Beilstein J. Org. Chem. 2020, 16, 1936–1946. doi:10.3762/bjoc.16.160
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Scholarly Works
- Leparfait, D.; Thierry, T.; da Rocha, N. L.; Legay, R.; Pfund, E.; Cormanich, R. A.; Lequeux, T. Stereoselective Ring-Opening Reaction of α-Fluorinated Oxetanes: A Practical and Theoretical Investigation. The Journal of organic chemistry 2024. doi:10.1021/acs.joc.4c01698
- Albitz, K.; Tóth, S.; Csókás, D.; Soós, T. Unlocking Oxetane Potential: Modular Synthetic Platform for the Concise Synthesis of Acyclic Oligo‐Isoprenoids and Terpenoids. Angewandte Chemie 2024. doi:10.1002/ange.202416441
- Albitz, K.; Tóth, S.; Csókás, D.; Soós, T. Unlocking Oxetane Potential: Modular Synthetic Platform for the Concise Synthesis of Acyclic Oligo-Isoprenoids and Terpenoids. Angewandte Chemie (International ed. in English) 2024, e202416441. doi:10.1002/anie.202416441
- Leparfait, D.; Xiao, F.; Coupri, D.; Gueulle, S.; Desriac, F.; Budin‐Verneuil, A.; Verneuil, N.; Hartke, A.; Pfund, E.; Lequeux, T. Oxetane Ring‐Opening Reaction: A Key Step for the Preparation of Substituted (Fluoro)alkenyl as Acyclonucleoside Mimics. European Journal of Organic Chemistry 2023, 26. doi:10.1002/ejoc.202300258
- Anaya, J.; Sánchez, R. M. Four-membered ring systems. Progress in Heterocyclic Chemistry; Elsevier, 2021; pp 53–91. doi:10.1016/b978-0-323-98410-2.00004-7