<i>N</i>-Aryl Lactams by Regioselective Ozonation of <i>N</i>-Aryl Cyclic Amines

<table>Plausible rearrangement mechanisms of aryl-morpholinyl hydrotrioxide intermediate formed by ozonation of 4-(4-nitrophenyl)morpholine (<b>3</b>). Pathway A leads to the formation of the corresponding lactame (<b>4</b>), pathway B to dehydro (<b>6</b>), diformyl (<b>7</b>), and dimeric (<b>8</b>) derivates.</table>

International Scholarly Research Notices

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Figure 3: <i>N</i>-Aryl Lactams by Regioselective Ozonation of <i>N</i>-Aryl Cyclic Amines 

International Scholarly Research Notices

N-Aryl Lactams by Regioselective Ozonation of N-Aryl Cyclic Amines

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