Supporting Information
| Supporting Information File 1: General experimental details, procedures, tabulated spectroscopic data, and 1H, 13C{1H}, and 19F NMR spectra of compounds 1g, 2a–i, and 3. | ||
| Format: PDF | Size: 1.2 MB | Download |
Cite the Following Article
Imide arylation with aryl(TMP)iodonium tosylates
Souradeep Basu, Alexander H. Sandtorv and David R. Stuart
Beilstein J. Org. Chem. 2018, 14, 1034–1038.
https://doi.org/10.3762/bjoc.14.90
How to Cite
Basu, S.; Sandtorv, A. H.; Stuart, D. R. Beilstein J. Org. Chem. 2018, 14, 1034–1038. doi:10.3762/bjoc.14.90
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.
Presentation Graphic
| Picture with graphical abstract, title and authors for social media postings and presentations. | ||
| Format: PNG | Size: 104.2 KB | Download |
Citations to This Article
Up to 20 of the most recent references are displayed here.
Scholarly Works
- Stuart, D. R. Synthesis of Aryl(TMP)iodonium Salts and Their Arylation Reactions. Synlett 2025, 36, 1669–1678. doi:10.1055/a-2564-5120
- Dohi, T.; Elboray, E. E.; Kikushima, K.; Morimoto, K.; Kita, Y. Iodoarene Activation: Take a Leap Forward toward Green and Sustainable Transformations. Chemical reviews 2025, 125, 3440–3550. doi:10.1021/acs.chemrev.4c00808
- Miyamoto, N.; Kikushima, K.; Sasa, H.; Katagiri, T.; Takenaga, N.; Kita, Y.; Dohi, T. Transition-metal-free dibenzoxazepinone synthesis by hypervalent iodine-mediated chemoselective arylocyclizations of N-functionalized salicylamides. Chemical communications (Cambridge, England) 2025, 61, 1882–1885. doi:10.1039/d4cc05908e
- Kiyokawa, K. 8 C—N Bond Forming Reactions with Hypervalent Iodine Reagents. Hypervalent Halogens in Organic Synthesis; Georg Thieme Verlag KG, 2025. doi:10.1055/sos-sd-246-00034
- Elboray, E. E.; Bae, T.; Kikushima, K.; Takenaga, N.; Kita, Y.; Dohi, T. Metal-Free Synthesis of Benzisoxazolones Utilizing ortho-Ester and ortho-Cyano-Functionalized Diaryliodonium Salts with Protected Hydroxylamines. The Journal of organic chemistry 2024, 89, 17518–17527. doi:10.1021/acs.joc.4c02242
- Kikushima, K.; Tsuda, T.; Miyamoto, N.; Kita, Y.; Dohi, T. Borate-mediated aryl polyfluoroalkoxylation under transition-metal-free conditions. Chemical communications (Cambridge, England) 2024, 60, 10552–10555. doi:10.1039/d4cc04008b
- Stuart, D. R. ACS In Focus; American Chemical Society, 2024. doi:10.1021/acsinfocus.7e8008
- Miyamoto, N.; Koseki, D.; Sumida, K.; Elboray, E. E.; Takenaga, N.; Kumar, R.; Dohi, T. Auxiliary strategy for the general and practical synthesis of diaryliodonium(III) salts with diverse organocarboxylate counterions. Beilstein journal of organic chemistry 2024, 20, 1020–1028. doi:10.3762/bjoc.20.90
- Stuart, D. R.; Gallagher, R. T.; Jha, S.; Metze, B. E. Synthesis of Alkyl Aryl Ethers by O-Arylation of Alcohols with Diaryliodonium Salts: Scope, Limitations, and Mechanism. Synlett 2023, 35, 889–894. doi:10.1055/a-2198-3637
- Radzhabov, A. D.; Soldatova, N. S.; Ivanov, D. M.; Yusubov, M. S.; Kukushkin, V. Y.; Postnikov, P. S. Metal-free and atom-efficient protocol for diarylation of selenocyanate by diaryliodonium salts. Organic & biomolecular chemistry 2023, 21, 6743–6749. doi:10.1039/d3ob00833a
- Kikushima, K.; Yamada, K.; Umekawa, N.; Yoshio, N.; Kita, Y.; Dohi, T. Decarboxylative arylation with diaryliodonium(iii) salts: alternative approach for catalyst-free difluoroenolate coupling to aryldifluoromethyl ketones. Green Chemistry 2023, 25, 1790–1796. doi:10.1039/d2gc04445e
- Soldatova, N. S.; Suslonov, V. V.; Ivanov, D. M.; Yusubov, M. S.; Resnati, G.; Postnikov, P. S.; Kukushkin, V. Y. Controlled Halogen-Bond-Involving Assembly of Double-σ-Hole-Donating Diaryliodonium Cations and Ditopic Arene Sulfonates. Crystal Growth & Design 2022, 23, 413–423. doi:10.1021/acs.cgd.2c01090
- Kikushima, K.; Kita, Y.; Dohi, T.; Morita, A.; Elboray, E. E.; Bae, T.; Miyamoto, N. Transition-Metal-Free N-Arylation of N-Methoxysulfonamides and N,O-Protected Hydroxylamines with Trimethoxyphenyliodonium (III) Acetates. Synthesis 2022, 54, 5192–5202. doi:10.1055/a-1922-8846
- Bugaenko, D. I.; Karchava, A. V. Catalyst‐Free Visible Light Mediated Synthesis of Unsymmetrical Tertiary Arylphosphines. Advanced Synthesis & Catalysis 2022, 364, 2248–2253. doi:10.1002/adsc.202200309
- Kikushima, K.; Elboray, E. E.; Jiménez-Halla, J. O. C.; Solorio-Alvarado, C. R.; Dohi, T. Diaryliodonium(III) salts in one-pot double functionalization of C-IIII and ortho C-H bonds. Organic & biomolecular chemistry 2022, 20, 3231–3248. doi:10.1039/d1ob02501e
- Kikushima, K.; Miyamoto, N.; Watanabe, K.; Koseki, D.; Kita, Y.; Dohi, T. Ligand- and Counterion-Assisted Phenol O-Arylation with TMP-Iodonium(III) Acetates. Organic letters 2022, 24, 1924–1928. doi:10.1021/acs.orglett.2c00294
- Soldatova, N. S.; Semenov, A. V.; Geyl, K. K.; Baykov, S. V.; Shetnev, A.; Konstantinova, A. S.; Korsakov, M. M.; Yusubov, M. S.; Postnikov, P. S. Copper-Catalyzed Selective N-Arylation of Oxadiazolones by Diaryliodonium Salts. Advanced Synthesis & Catalysis 2021, 363, 3566–3576. doi:10.1002/adsc.202100426
- Nilova, A.; Metze, B.; Stuart, D. R. Aryl(TMP)iodonium Tosylate Reagents as a Strategic Entry Point to Diverse Aryl Intermediates: Selective Access to Arynes. Organic letters 2021, 23, 4813–4817. doi:10.1021/acs.orglett.1c01534
- Saikia, R. A.; Barman, D.; Dutta, A.; Thakur, A. J. N1‐ and N3‐Arylations of Hydantoins Employing Diaryliodonium Salts via Copper(I) Catalysis at Room Temperature. European Journal of Organic Chemistry 2020, 2021, 400–410. doi:10.1002/ejoc.202001353
- Raviola, C.; Protti, S. Leaving Groups in Metal-Free Arylations: Make Your Choice!. European Journal of Organic Chemistry 2020, 2020, 5292–5304. doi:10.1002/ejoc.202000143