Abstract
Oxypalmatine and oxypseudopalmatine were synthesized in three steps from the benzonitrile 11 and toluamides 12a, b. The lithiated cycloaddition reaction yielded 3-arylisoquinolinone intermediates. A subsequent internal SN2 reaction produced the corresponding 8-oxoprotoberberines, oxypalmatine and oxypseudopalmatine.
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Thanh, N. L., & Cho, W. J. (2007). Novel synthesis of the natural protoberberine alkaloids: Oxypalmatine and oxypseudopalmatine. Bulletin of the Korean Chemical Society, 28(5), 763–766. https://doi.org/10.5012/bkcs.2007.28.5.763
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