tedanolide-c has been researched along with 3-hydroxybutanal* in 1 studies
1 other study(ies) available for tedanolide-c and 3-hydroxybutanal
Article | Year |
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A Kiyooka aldol approach for the synthesis of the C(14)-C(23) segment of the diastereomeric analog of tedanolide C.
The challenging synthesis of a quaternary center within the highly oxygenated setting of tedanolide C can be performed via a Kiyooka aldol reaction. Here, the diastereomeric analog of tedanolide C with the configurations between C10 and C20 opposite compared to the proposed structure was chosen as the synthetic target. The tetra-substituted silyl ketene acetal provides the southern hemisphere of tedanolide C in useful selectivities, and the absolute configuration of the newly generated quaternary center was determined by NOE experiments of the corresponding acetonide. Topics: Aldehydes; Carbon; Ketones; Macrolides; Molecular Structure; Stereoisomerism | 2011 |