Application |
- 1. [2+3]-dipolar cycloaddition of cyclic enones.
- 2. Activation of α,β-unsaturated carbonyl compounds:
- a) vinylogous α-ketol rearrangement.
- b) vinylogous Michael addition of β-substituted α,β-unsaturated cyclohexanones.
- 3. Michael addition
- a) α-nitroacetate to α,β-unsaturated ketones.
- b) Diastereodivergent Michael addition to α-substituted, α,β-unsaturated ketones.
- 4. α-benzoyloxylation of α-branched aldehydes.
- 5. [4+2]-cycloadditions of β-substituted α,β-unsaturated cyclohexanones with polyconjugated malonitriles.
- 6. Vinylogous organocascade catalysis with control of remote stereochemistry in the synthesis of spirocyclic oxindoles.
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