Institut für Organische Chemie, Johannes Gutenberg-Universität, Duesbergweg 10-14, 55128 Mainz (Germany) http://www.chemie.uni-mainz.de/OC/AK-Waldvogel/.
Institut für Organische Chemie, Johannes Gutenberg-Universität, Duesbergweg 10-14, 55128 Mainz (Germany) http://www.chemie.uni-mainz.de/OC/AK-Waldvogel/
Angew Chem Int Ed Engl. 2015 May 26;54(22):6398-9. doi: 10.1002/anie.201502638. Epub 2015 May 12.
Simply by applying electricity, the amination reaction of a broad variety of arenes, heteroarenes, and benzylic substrates is achieved. Pyridine serves as the nitrogen source and the intermediate cationic species are well-protected from over-oxidation.
通过施加电流,实现了广泛的芳烃、杂芳烃和苄基底物的胺化反应。吡啶作为氮源,中间阳离子物种得到很好的保护,避免了过度氧化。