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.
Author supplied keywords
Cite
CITATION STYLE
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
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.