Self-Assembly of Disorazole C1 through a One-Pot Alkyne Metathesis Homodimerization Strategy

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Abstract

Abstract Alkyne metathesis is increasingly explored as a reliable method to close macrocyclic rings, but there are no prior examples of an alkyne-metathesis-based homodimerization approach to natural products. In this approach to the cytotoxic C2-symmetric marine-derived bis(lactone) disorazole C1, a highly convergent, modular strategy is employed featuring cyclization through an ambitious one-pot alkyne cross-metathesis/ring-closing metathesis self-assembly process.

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Ralston, K. J., Ramstadius, H. C., Brewster, R. C., Niblock, H. S., & Hulme, A. N. (2015). Self-Assembly of Disorazole C1 through a One-Pot Alkyne Metathesis Homodimerization Strategy. Angewandte Chemie - International Edition, 54(24), 7086–7090. https://doi.org/10.1002/anie.201501922

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