Abstract
The development of an intramolecular vicinal diamination protocol using metalfree conditions is discussed. The reaction uses a bromide source to generate a Br(I) catalyst in situ from a benign terminal oxidant such as sodium chlorite. The reaction is of great scope and surpasses the transition-metal catalyses developed so far for these types of reactions. © 2013 IUPAC.
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APA
Muñiz, K. (2013). Metal-free catalytic vicinal diamination of alkenes. Pure and Applied Chemistry, 85(4), 755–761. https://doi.org/10.1351/PAC-CON-12-10-23
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