Photoiodization of toluene in a microflow platform
Author:
Funder
National Natural Science Foundation of China
Publisher
Springer Science and Business Media LLC
Subject
Organic Chemistry,Fluid Flow and Transfer Processes,Chemistry (miscellaneous)
Link
https://link.springer.com/content/pdf/10.1007/s41981-021-00187-w.pdf
Reference40 articles.
1. Li L, Liu W, Mu X, Mi Z, Li C-J (2016) Photo-induced iodination of aryl halides under very mild conditions. Nat Protoc 11(10):1948–1954. https://doi.org/10.1038/nprot.2016.125
2. Ling X-G, Xiong Y, Zhang S-T, Huang R-F, Zhang X-H (2013) Effective synthesis of benzyl halides triggered by in situ prepared hypervalent halides. Chin Chem Lett 24(1):45–48. https://doi.org/10.1016/j.cclet.2012.12.013
3. Montoro R, Wirth T (2005) Direct bromination and iodination of non-activated alkanes by hypohalite reagents. Synthesis-Stuttgart (9):1473–1478. https://doi.org/10.1055/s-2005-865322
4. Artaryan A, Mardyukov A, Kulbitski K, Avigdori I, Nisnevich GA, Schreiner PR, Gandelman M (2017) Aliphatic C-H bond iodination by a N-iodoamide and isolation of an elusive N-amidyl radical. J Org Chem 82(14):7093–7100. https://doi.org/10.1021/acs.joc.7b00557
5. Stavber S, Jereb M, Zupan M (2008) Electrophilic iodination of organic compounds using elemental iodine or iodides. Synthesis-Stuttgart 10:1487–1513. https://doi.org/10.1055/s-2008-1067037
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