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- W2115354588 abstract "(1R*,2S*)-2-(2-Oxobut-3-enyl)-1-(1-oxoprop-2-enyl)-1,3,3-trimethylcyclopentane 5 was prepared stereoselectively from 4,4-dimethylcyclopent-2-en-1-one 6 and then converted into the conjugated silyl enol ether 17. Intramolecular cycloaddition of 17, followed by base-catalysed equilibration, provided (1S*,2R*,7R*,9R*)-3-tert-butyldimethylsiloxy-9,12,12-trimethyltricyclo[7.3.0.0]dodec-3-en-8-one 18a, which was transformed, after contraction of the cyclohexene ring, into the synthetic intermediate 32 for (±)-Δ9(12)-capnellene 1." @default.
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- W2115354588 date "1992-01-01" @default.
- W2115354588 modified "2023-10-10" @default.
- W2115354588 title "Stereoselective construction of cis-transoid-cis-tricyclo[7.3.0.0]dodecanes by an intramolecular Diels–Alder reaction: a formal total synthesis of (±)-Δ<sup>9(12)</sup>-capnellene" @default.
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- W2115354588 doi "https://doi.org/10.1039/p19920000865" @default.
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