Cite the Following Article
Stereoselective α-fluoroamide and α-fluoro-γ-lactone synthesis by an asymmetric zwitterionic aza-Claisen rearrangement
Kenny Tenza, Julian S. Northen, David O'Hagan and Alexandra M. Z. Slawin
Beilstein J. Org. Chem. 2005, 1, No. 13.
https://doi.org/10.1186/1860-5397-1-13
How to Cite
Tenza, K.; Northen, J. S.; O'Hagan, D.; Slawin, A. M. Z. Beilstein J. Org. Chem. 2005, 1, No. 13. doi:10.1186/1860-5397-1-13
Download Citation
Citation data can be downloaded as file using the "Download" button or used for copy/paste from the text window
below.
Citation data in RIS format can be imported by all major citation management software, including EndNote,
ProCite, RefWorks, and Zotero.
Citations to This Article
Up to 20 of the most recent references are displayed here.
Scholarly Works
- Li, T.-P.; Li, R.-S.; Hu, W.; Xie, J.-X.; Xu, M.; Feng, C.; Ni, H.-L.; Yu, W.-H.; Hu, P.; Wang, B.-Q.; Cao, P. Modular Synthesis of Enantioenriched α-Chiral Homoallylic Amidines Enabled by Relay Ir/Cu Catalysis. Organic letters 2022, 24, 6783–6788. doi:10.1021/acs.orglett.2c02655
- Liu, A.; Ni, C.; Xie, Q.; Hu, J. TMSCF2 Br-Enabled Fluorination-Aminocarbonylation of Aldehydes: Modular Access to α-Fluoroamides. Angewandte Chemie (International ed. in English) 2021, 61, e202115467. doi:10.1002/anie.202115467
- Liu, A.; Ni, C.; Xie, Q.; Hu, J. TMSCF2Br‐Enabled Fluorination–Aminocarbonylation of Aldehydes: Modular Access to α‐Fluoroamides. Angewandte Chemie 2021, 134. doi:10.1002/ange.202115467
- Dai, R.-H.; Wang, Q.; Chen, Z.-X.; Tian, S.-K. Asymmetric Aza-Claisen Rearrangement between Enantioenriched α-Chiral Allylamines and Allenones. The Journal of organic chemistry 2021, 86, 3065–3073. doi:10.1021/acs.joc.0c02721
- Christmann; Paquin; Weinreb; Carreira; Schaumann. Knowledge Updates: 2017/2 - 34.1.6.4 Synthesis of Fluoroalkanes with Retention of the Functional Group (Update 2017). Knowledge Updates 2017/2; Georg Thieme Verlag KG, 2017. doi:10.1055/sos-sd-134-00125
- Wang, J.-X.; Wu, J.-J.; Chen, H.; Zhang, S.; Wu, F. Synthesis of difluoroalkyl-γ-butyrolactones from iododifluoromethyl ketones and 4-pentenoic acids. Chinese Chemical Letters 2015, 26, 1381–1384. doi:10.1016/j.cclet.2015.07.007
- Phae-nok, S.; Soorukram, D.; Kuhakarn, C.; Reutrakul, V.; Pohmakotr, M. Silver-Mediated Decarboxylative Fluorination of Paraconic Acids: A Direct Entry to β-Fluorinated γ-Butyrolactones. European Journal of Organic Chemistry 2015, 2015, 2879–2888. doi:10.1002/ejoc.201500023
- Silla, J. M.; Silva, W. G. D. P.; Cormanich, R. A.; Rittner, R.; Tormena, C. F.; Freitas, M. P. Gauche preference of β-fluoroalkyl ammonium salts. The journal of physical chemistry. A 2014, 118, 503–507. doi:10.1021/jp410458w
- Majumdar, K.; Bhattacharyya, T. doi:10.1002/9780470638859.conrr029
- Lam, Y.-h.; Stanway, S. J.; Gouverneur, V. Recent progress in the use of fluoroorganic compounds in pericyclic reactions. Tetrahedron 2009, 65, 9905–9933. doi:10.1016/j.tet.2009.08.005
- Tredwell, M.; Luft, J.; Schuler, M.; Tenza, K.; Houk, K.; Gouverneur, V. Fluorine‐Directed Diastereoselective Iodocyclizations. Angewandte Chemie 2007, 120, 363–366. doi:10.1002/ange.200703465
- Tredwell, M.; Luft, J. A. R.; Schuler, M.; Tenza, K.; Houk, K. N.; Gouverneur, V. Fluorine-directed diastereoselective iodocyclizations. Angewandte Chemie (International ed. in English) 2007, 47, 357–360. doi:10.1002/anie.200703465
- Gooseman, N. E. J.; O'Hagan, D.; Peach, M. J. G.; Slawin, A. M. Z.; Tozer, D. J.; Young, R. J. An electrostatic gauche effect in beta-fluoro- and beta-hydroxy-N-ethylpyridinium cations. Angewandte Chemie (International ed. in English) 2007, 46, 5904–5908. doi:10.1002/anie.200700714
- Gooseman, N.; O'Hagan, D.; Peach, M.; Slawin, A.; Tozer, D.; Young, R. An Electrostatic Gauche Effect in β‐Fluoro‐ and β‐Hydroxy‐N‐ethylpyridinium Cations. Angewandte Chemie 2007, 119, 6008–6012. doi:10.1002/ange.200700714
