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Journal Article

Toward the total synthesis of spirastrellolide A. Part 3: Intelligence gathering and preparation of a ring-expanded analogue

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

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

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O'Neil,  Gregory W.
Research Department Fürstner, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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Fenster,  Michaël D. B.
Research Department Fürstner, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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

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

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Supplementary Material (public)

b707835h.pdf
(Supplementary material), 242KB

b707835h1.pdf
(Supplementary material), 3MB

Citation

Fürstner, A., Fasching, B., O'Neil, G. W., Fenster, M. D. B., Godbout, C., & Ceccon, J. (2007). Toward the total synthesis of spirastrellolide A. Part 3: Intelligence gathering and preparation of a ring-expanded analogue. Chemical Communications, (29), 3045-3047. doi:10.1039/B707835H.


Cite as: https://hdl.handle.net/11858/00-001M-0000-0025-ACF5-4
Abstract
Different methods for the formation of the C.25–C.26 bond of spirastrellolide A (1) are evaluated that might qualify for the end game of the projected total synthesis, with emphasis on metathetic ways to forge the macrocyclic frame.