Abstract
The synthesis of complex natural products serves as a source of great inspiration and challenge for organic chemists. The synthesis of strychnine is no exception. With six contiguous stereocenters, five of which adorn the central cyclohexane ring, a stereodefined trisubstituted olefin, and seven rings, strychnine (1, Fig. 4.1) presents a significant challenge for synthesis.
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CITATION STYLE
Martin, D. B. C., & Vanderwal, C. D. (2012). A short synthesis of strychnine from pyridine. In Total Synthesis of Natural Products: At the Frontiers of Organic Chemistry (Vol. 9783642340659, pp. 67–102). Springer-Verlag Berlin Heidelberg. https://doi.org/10.1007/978-3-642-34065-9_4
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