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Journal Article

Second-Generation Total Synthesis of Spirastrellolide F Methyl Ester: The Alkyne Route

MPS-Authors
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Benson,  Stefan
Research Department Fürstner, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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Collin,  Marie-Pierre
Research Department Fürstner, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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Arlt,  Alexander
Research Department Fürstner, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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Gabor,  Barbara
Service Department Farès (NMR), Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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Goddard,  Richard
Service Department Lehmann (EMR), Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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Fürstner,  Alois
Research Department Fürstner, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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Supplementary Material (public)

anie_201103270_sm_miscellaneous_information.pdf
(Supplementary material), 3MB

Citation

Benson, S., Collin, M.-P., Arlt, A., Gabor, B., Goddard, R., & Fürstner, A. (2011). Second-Generation Total Synthesis of Spirastrellolide F Methyl Ester: The Alkyne Route. Angewandte Chemie International Edition, 50(37), 8739-8744. doi:10.1002/anie.201103270.


Cite as: https://hdl.handle.net/11858/00-001M-0000-0014-CA40-1
Abstract
Outlandish: The spiroketal embedded in spirastrellolide F methyl ester is a daring site for ring closure, yet it has allowed the power of catalytic alkyne scission and activation to be showcased. An improved strategy for the introduction of the labile side chain was also developed.