Abstract
The reactions of phosphorylated 2-nitro-and 2-bromo-2-nitroethenes with sodium azide involve 1,3-dipolar cycloaddition to form triazoles, aziridines and isomeric vinyl azides. The latter products were isolated as a mixture of structural isomers. The structure of the obtained compounds was determined by IR and 1H and 31P NMR spectroscopy.
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