Aromatic C-H Bond Functionalization Induced by Electrochemically in Situ Generated Tris(p-bromophenyl)aminium Radical Cation: Cationic Chain Reactions of Electron-Rich Aromatics with Enamides.
- DOI
- 10.1021/acs.joc.5b02222
- Published
- 2015 Nov 6
- Container
- The Journal of organic chemistry
- Publisher
- Not recorded
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1021/acs.joc.5b02222,
title = {Aromatic C-H Bond Functionalization Induced by Electrochemically in Situ Generated Tris(p-bromophenyl)aminium Radical Cation: Cationic Chain Reactions of Electron-Rich Aromatics with Enamides.},
author = {Li LJ and Jiang YY and Lam CM and Zeng CC and Hu LM and Little RD},
year = {2015},
journal = {The Journal of organic chemistry},
doi = {10.1021/acs.joc.5b02222},
url = {https://doi.org/10.1021/acs.joc.5b02222}
}RIS
TY - JOUR TI - Aromatic C-H Bond Functionalization Induced by Electrochemically in Situ Generated Tris(p-bromophenyl)aminium Radical Cation: Cationic Chain Reactions of Electron-Rich Aromatics with Enamides. AU - Li LJ AU - Jiang YY AU - Lam CM AU - Zeng CC AU - Hu LM AU - Little RD PY - 2015 JO - The Journal of organic chemistry DO - 10.1021/acs.joc.5b02222 UR - https://doi.org/10.1021/acs.joc.5b02222 ER -
APA
LJ, L., YY, J., CM, L., CC, Z., LM, H., & RD, L. (2015). Aromatic C-H Bond Functionalization Induced by Electrochemically in Situ Generated Tris(p-bromophenyl)aminium Radical Cation: Cationic Chain Reactions of Electron-Rich Aromatics with Enamides.. The Journal of organic chemistry. https://doi.org/10.1021/acs.joc.5b02222
Source records
- pubmed · retrieved 2026-09-27T15:57:22.419Z