Journal
HETEROCYCLES
Volume 53, Issue 3, Pages 519-+Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.3987/COM-99-8749
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Electrochemical oxidations of 1-tosyl-3-aryl-1,3-diazadihydroazulanones gave 6-tosyl-3-aryl-1,3-diazadihydroazulanones via migrations of the tosyl group. On the other hand, electrochemical reductions of the 1-tosylazulanones afforded 3-aryl-1,3-diazadihydroazulanones through eliminations of the tosyl group.
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