Supporting Information
| Supporting Information File 1: Experimental details, crystallographic data (selected intermolecular bond lengths) as well as a description of the 19F NMR monitoring experiments and data analysis. | ||
| Format: PDF | Size: 533.8 KB | Download |
Cite the Following Article
Synthesis, characterization and initial evaluation of 5-nitro-1-(trifluoromethyl)-3H-1λ3,2-benziodaoxol-3-one
Nico Santschi, Roman C. Sarott, Elisabeth Otth, Reinhard Kissner and Antonio Togni
Beilstein J. Org. Chem. 2014, 10, 1–6.
https://doi.org/10.3762/bjoc.10.1
How to Cite
Santschi, N.; Sarott, R. C.; Otth, E.; Kissner, R.; Togni, A. Beilstein J. Org. Chem. 2014, 10, 1–6. doi:10.3762/bjoc.10.1
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
- Kumar, R.; Dohi, T.; Zhdankin, V. V. Organohypervalent heterocycles. Chemical Society reviews 2024, 53, 4786–4827. doi:10.1039/d2cs01055k
- Yoshimura, A.; Saito, A.; Zhdankin, V. V. Recent Progress in Synthetic Applications of Cyclic Hypervalent Iodine(III) Reagents. Advanced Synthesis & Catalysis 2023, 365, 2653–2675. doi:10.1002/adsc.202300275
- Robidas, R.; Legault, C. Y. Cyclic Haloiodanes: Syntheses, Applications and Fundamental Studies. Helvetica Chimica Acta 2021, 104. doi:10.1002/hlca.202100111
- Kalim, J.; Duhail, T.; Le, T.-N.; Vanthuyne, N.; Anselmi, E.; Togni, A.; Magnier, E. Merging hypervalent iodine and sulfoximine chemistry: a new electrophilic trifluoromethylation reagent. Chemical science 2019, 10, 10516–10523. doi:10.1039/c9sc04289j
- Xu, C.; Huang, W.; Zhang, R.; Gao, C.; Li, Y.; Wang, M. Trifluoromethylations of Alkenes Using PhICF3Cl as Bifunctional Reagent. The Journal of organic chemistry 2019, 84, 14209–14216. doi:10.1021/acs.joc.9b01901
- Kawamura, S.; Sodeoka, M. Fluoroalkylation Methods for Synthesizing Versatile Building Blocks. Bulletin of the Chemical Society of Japan 2019, 92, 1245–1262. doi:10.1246/bcsj.20190080
- Jiang, H.; Sun, T.-Y.; Chen, Y.; Zhang, X.; Wu, Y.-D.; Xie, Y.; Schaefer, H. F. Designing new Togni reagents by computation. Chemical communications (Cambridge, England) 2019, 55, 5667–5670. doi:10.1039/c9cc01320b
- Wu, Y.; Shafir, A. PATAI'S Chemistry of Functional Groups - NMR of Hypervalent Iodine Compounds. Patai's Chemistry of Functional Groups 2018, 1–33. doi:10.1002/9780470682531.pat0942
- Liebing, P.; Pietrasiak, E.; Otth, E.; Kalim, J.; Bornemann, D.; Togni, A. Supramolecular Aggregation of Perfluoroorganyl Iodane Reagents in the Solid State and in Solution. European Journal of Organic Chemistry 2018, 2018, 3771–3781. doi:10.1002/ejoc.201800358
- Li, M.; Zheng, H.; Xue, X.-S.; Cheng, J.-P. Ordering the relative power of electrophilic fluorinating, trifluoromethylating, and trifluoromethylthiolating reagents: A summary of recent efforts. Tetrahedron Letters 2018, 59, 1278–1285. doi:10.1016/j.tetlet.2018.02.039
- Santschi, N.; Nauser, T. Rate of single electron reduction of Togni’s reagent. Journal of Fluorine Chemistry 2017, 203, 218–222. doi:10.1016/j.jfluchem.2017.03.003
- Kawamura, S.; Sekine, D.; Sodeoka, M. Synthesis of CF3-containing oxazolines via trifluoromethylation of allylamides with Togni reagent in the presence of alkali metal iodides. Journal of Fluorine Chemistry 2017, 203, 115–121. doi:10.1016/j.jfluchem.2017.07.012
- Pietrasiak, E.; Togni, A. Synthesis and Characterization of Fluorinated Hypervalent Tellurium Derivatives. Organometallics 2017, 36, 3750–3757. doi:10.1021/acs.organomet.7b00535
- Umemoto, T. Development of Electrophilic Trifluoromethylating Reagents. Modern Synthesis Processes and Reactivity of Fluorinated Compounds; Elsevier, 2017; pp 265–287. doi:10.1016/b978-0-12-803740-9.00010-x
- Li, M.; Xue, X.-S.; Guo, J.; Wang, Y.; Cheng, J.-P. An Energetic Guide for Estimating Trifluoromethyl Cation Donor Abilities of Electrophilic Trifluoromethylating Reagents: Computations of X–CF3 Bond Heterolytic Dissociation Enthalpies. The Journal of organic chemistry 2016, 81, 3119–3126. doi:10.1021/acs.joc.5b02821
- Yoshimura, A.; Zhdankin, V. V. Advances in Synthetic Applications of Hypervalent Iodine Compounds. Chemical reviews 2016, 116, 3328–3435. doi:10.1021/acs.chemrev.5b00547
- Sala, O.; Santschi, N.; Jungen, S.; Lüthi, H. P.; Iannuzzi, M.; Hauser, N.; Togni, A. S‐Trifluoromethylation of Thiols by Hypervalent Iodine Reagents: A Joint Experimental and Computational Study. Chemistry (Weinheim an der Bergstrasse, Germany) 2016, 22, 1704–1713. doi:10.1002/chem.201503774
- Zhu, H.; Zhang, S.; Wang, H.; Xu, B.; Guo, Y. Study on the Degradation of the Highly Reactive Hypervalent Trifluoromethylation Iodine Reagent PhI(OAc)(CF3). Chinese Journal of Chemistry 2015, 33, 1365–1370. doi:10.1002/cjoc.201500730
- Früh, N.; Charpentier, J.; Togni, A. Iodanes as Trifluoromethylation Reagents. Topics in current chemistry 2015, 373, 167–186. doi:10.1007/128_2015_658
- Ling, L.; Liu, K.; Li, X.; Li, Y. General Reaction Mode of Hypervalent Iodine Trifluoromethylation Reagent: A Density Functional Theory Study. ACS Catalysis 2015, 5, 2458–2468. doi:10.1021/cs501892s
