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Cite the Following Article
A novel methodology for the efficient synthesis of 3-monohalooxindoles by acidolysis of 3-phosphate-substituted oxindoles with haloid acids
Li Liu, Yue Li, Tiao Huang, Dulin Kong and Mingshu Wu
Beilstein J. Org. Chem. 2021, 17, 2321–2328.
https://doi.org/10.3762/bjoc.17.150
How to Cite
Liu, L.; Li, Y.; Huang, T.; Kong, D.; Wu, M. Beilstein J. Org. Chem. 2021, 17, 2321–2328. doi:10.3762/bjoc.17.150
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- Bałczewski, P.; Owsianik, K. Quinquevalent phosphorus acids. Organophosphorus Chemistry; Royal Society of Chemistry, 2024; pp 109–231. doi:10.1039/bk9781837672738-00109
- Zheng, Y.; Lu, W.; Ma, T.; Huang, S. SO2ClF‐Promoted Chlorooxidation of Tryptamine Derivatives: Synthesis of 3,3‐Disubstituted Oxindoles. Asian Journal of Organic Chemistry 2023, 13. doi:10.1002/ajoc.202300552
- Wells, C. E.; Ramos, L. P.; Harstad, L. J.; Hessefort, L. Z.; Lee, H. J.; Sharma, M.; Biegasiewicz, K. F. Decarboxylative Bromooxidation of Indoles by a Vanadium Haloperoxidase. ACS Catalysis 2023, 13, 4622–4628. doi:10.1021/acscatal.2c05531
- Ma, T.; Zheng, Y.; Huang, S. SO2ClF: A Reagent for Controllable Chlorination and Chlorooxidation of Simple Unprotected Indoles. The Journal of organic chemistry 2023, 88, 4839–4847. doi:10.1021/acs.joc.3c00039
- Jian, Y.; Liang, P.; Li, X.; Shao, H.; Ma, X. Controllable transformation of indoles using iodine(III) reagent. Organic & biomolecular chemistry 2022, 21, 179–186. doi:10.1039/d2ob01951e
- Li, Y.; Liu, L.; Wang, F.; Ning, R.; Kong, D.; Wu, M. Solvent‐free Darzens condensation of 3‐chlorooxindoles with aryl aldehydes for diastereoselective construction of spiro‐epoxyoxindoles by grinding. Journal of Heterocyclic Chemistry 2022, 60, 692–699. doi:10.1002/jhet.4606
