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Pyrrolo[3,4-b]indoles 8 are conveniently synthesized from 2,3-dimethylindole (4) in four steps, the last of which is DDQ oxidation of dihydropyrrolo[3,4-b]indoles 7 (85–98% yield).
This investigation was supported by the National Institutes of Health (GM58601), for which support we are grateful.
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