Abstract
No bones about it: (-)-Norzoanthamine, a promising candidate for an anti-osteoporotic drug, was the target of a total synthesis (see scheme). The final bisaminal formation with AcOH/H2O gave the DEFG ring, while the cyclization precursor was prepared by installing the remaining bisaminal unit after oxidative cleavage of the cyclopentanol moiety. © 2009 Wiley-VCH Verlag GmbH & Co. KGaA.
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Yamashita, D., Murata, Y., Hikage, N., Takao, K. I., Nakazaki, A., & Kobayashi, S. (2009). Total synthesis of (-)-norzoanthamine. Angewandte Chemie - International Edition, 48(8), 1404–1406. https://doi.org/10.1002/anie.200804546
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