Abstract
We have studied the reaction of 10-methyl(phenyl)-5,10-dihydrophenarsazine 10-oxides with hydriodic acid and we have established the structure of the products by high-resolution mass spectrometry. We have shown that when the methyl group is replaced by a phenyl group in 5,10-dihydrophenarsazine 10-oxides, cleavage of the endocyclic arsenic–carbon bonds occurs.
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Gavrilov, V.I., Karavanov, A.A., Musin, R.R. et al. Reaction of 10-Methyl(phenyl)-5,10-dihydrophenarsazine 10-Oxides with Hydriodic Acid. Chemistry of Heterocyclic Compounds 40, 1212–1215 (2004). https://doi.org/10.1023/B:COHC.0000048297.35826.d3
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DOI: https://doi.org/10.1023/B:COHC.0000048297.35826.d3