Abstract
1. Aminofurazans are fluorinated by elemental fluorine selectively at the amino group with the formation of N,N-difluoroamino derivatives as the main products. The reaction can be accompanied by oxidative dimerization to the corresponding azo compounds. 2. The difluoroamino group in a series of furazans exhibits the properties of an R substituent.
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More From: Bulletin of the Academy of Sciences of the USSR Division of Chemical Science
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