terpestacin has been researched along with cyclopentenone* in 1 studies
1 other study(ies) available for terpestacin and cyclopentenone
Article | Year |
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Terpestacin core structure. control of stereochemistry.
[reaction: see text] The alpha-hydroxycyclopentenone core structure of terpestacin has been prepared in a model system through an allene ether Nazarov cyclization of an alkylidene-gamma-butyrolactone followed by regio- and stereoselective alkylation reactions. The stereochemistry at C15 (terpestacin numbering) has been used to control stereochemistry at C1 and at C23. The use of E-alkylidene-gamma-butyrolactones extends the scope of the cationic cyclopentannelation reaction. Topics: Alkylation; Bridged Bicyclo Compounds; Cyclopentanes; Molecular Structure; Stereoisomerism | 2005 |