Issue 17, 1998

Squalestatin synthetic studies: tethered control in a bicycloketalisation step

Abstract

A synthesis of an analogue of the dioxabicyclo[3.2.1]octane core structure of the squalestatins is reported in which control of the bicycloketalisation is achieved by a tethering strategy.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1998, 2795-2802

Squalestatin synthetic studies: tethered control in a bicycloketalisation step

A. M. Reid and P. G. Steel, J. Chem. Soc., Perkin Trans. 1, 1998, 2795 DOI: 10.1039/A804233K

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