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Three highly substituted cyclo­hexa­nols were prepared in satisfactory yield and with good stereospecificity by reaction of 4-halogenobenzaldehydes with 2-acetyl­pyridine under mild conditions. The mol­ecular structures of the cyclo­hexa­nols are very similar, but the crystal structures, particularly the space groups and the supra­molecular assemblies, are all different.
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