A general approach for the stereoselective synthesis of conduritols A 1, (+)-C 3 and (–)-C 3 starting from D-galactose is described. The utility of the key cyclohexenone intermediate 11 leading to the synthesis of conduritols 1, (+)-3 and (–)-3 by straightforward synthetic manipulations is described.
H. B. Mereyala and B. R. Gaddam, J. Chem. Soc., Perkin Trans. 1, 1994, 2187 DOI: 10.1039/P19940002187
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