Journal
GREEN CHEMISTRY
Volume 19, Issue 24, Pages 5940-5948Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c7gc03141f
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Funding
- research council of the University of Guilan
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tert-Amines were harnessed to afford arenesulfonyl hydrazides and arenesulfonyl chlorides via a metal-, oxidant-and halogen-free electrochemical oxidative coupling in an undivided cell at RT. This environmentally benign approach afforded a wide spectrum of sulfonamides in satisfactory yields using cheap and renewable Pencil Graphite Electrodes (PGEs).
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